Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: MQF FDA class 2

Catheter, Assisted Reproduction

Obstetrics/Gynecology

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The Assisted Reproduction Catheter is an obstetrics/gynecology device used in ART procedures such as embryo transfer or intrauterine insemination, designed for the gentle and precise delivery of gametes or embryos into the uterine cavity. Classified as FDA Class 2 under 21 CFR 884.6110, it requires 510(k) premarket notification. The product code is MQF, and it is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)
FemaSeed Intratubal Insemination
Daylily Single Use Sterile Embryo Transfer Catheter
Allwin Embryo Transfer Catheters (ETC), Allwin ETC Stylets and Soft Obturators
Kitazato ET Catheters
Allwin Intra Uterine Insemination Catheters (INSEMINA and INSEMINA Open Tip Intra Uterine Insemination Catheter, CURVED and CURVED Open Tip Intra Uterine Insemination Catheter, TRACKABLE and TRACKABLE Open Tip Intra Uterine Insemination Catheter, FLEXI and FLEXI Open Tip Intra Uterine Insemination Catheter, STUMPY Intra Uterine Insemination Catheter)
Soft-Pass Embryo Mock Transfer Catheter Sets (Soft-Pass Embryo Mock Transfer Catheter Set and Soft-Pass Embryo Mock Transfer Catheter Set with Echogenic Tip)
Guardia™ Access Malleable Obturator, Guardia™ Obturator, Soft-Pass™ Obturator, Soft-Trans Malleable Obturator, Guardia™ ETS Embryo-Tested Syringe, Flushing Catheter
Towako Transmyometrial Embryo Transfer Set
Pivet and Soft-Pass Embryo Transfer Catheter Sets
Guardia Access Embryo Transfer Catheter Sets and Sydney IVF® Transfer Catheter
Guardia™ Access Nano and Soft-Trans Embryo Transfer Catheter Sets, Soft-Trans Embryo Transfer Catheter, Soft-Trans Guide Catheter
Shepard, Insemi-Cath, and Soft-Pass Coaxial - Cook Intrauterine Insemination Catheters
Soules Intrauterine Insemination Catheter
Kitazato ET Catheters
Kitazato IUI Catheter
Transem and EchoGen Embryo Transfer Catheters
CrossBay IVF Embryo Transfer Catheter Set
MedGyn Straight IUI Catheter, MedGyn Mini IUI Catheter, MedGyn curved, mini IUI Catheter
FERTILIGENT SLOW RELEASE IUI CATHETER KIT
KITAZATO IUI CATHETER
IUI CATHETERS
INTRAUTERINE INSEMINATION (IUI) CATHETER
INTRAUTERINE INSEMINATION (IUI) CATHETER
CLEAR VISION EMBRYO TRANSFER CATHETER SET, MODEL B100000 - B 100007; CLEAR VISION TRIAL TRANSFER CATHETER SET
IUI CATHETER, MODEL 9057
EMBRYO TRANSFER CATHETER WITH ACCESSORY STYLET, MODELS 9018, 9023, 9018-S, 9023-S
MORTON IUI CATHETERS
WALLACE (SURE VIEW) EMBRYO REPLACEMENT CATHETER AND TRIAL TRANSFER CATHETER
COOPERSURGICAL MALLEABLE SYTLET
COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER
TUCKER EMBRYO CATHETER
COOPERSURGICAL TRIAL TRANSFER CATHETER
COOPERSURGICAL EMBRYO TRANSFER CATHETER, COOPERSURGICAL ASSISTED REPRODUCTION CATHETER
IUI, MODEL 4220; SMOOZE, MODEL 4225, L; SEMINOR, MODEL 4502 A, B
EMTRAC; DELPHIN; SEMTRAC 2000 SET
TAO EMBRYO TRANSFER CATHETER SYSTEM
EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201
EMBRYON GIFT TRANSFER CATHETERS/SETS
EMBRYON TRANSFER CATHETERS/SETS
EMBRYO GLIDE EMBRYO TRANSFER CATHETER, EMBRYO GLIDE STYLE FOR EMBRYO TRANSFER CATHETER
<GENX> EMBRYO TRANSFER CATHETER CC GLIDER
WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N
WALLACE MALLEABLE STYLET-18CM, MODEL 1816ST, WALLACE MALLEABLE STYLET-23CM, MODEL 1816NST
WALLACE CATHETERS-18CM, MODEL 1816; 23CM, MODEL 1816N; 23CM, MODEL 2316
INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER
TRANSMYOMETRIAL EMBRYO TRANSFER SET
INTRATUBAL TRANSFER SETS
GIFT CATHETER SET/S
EMBRYO TRANSFER CATHETERS/SETS

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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