FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM

K Number: K953314 · Decision Jul 28, 1995
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
4
Applicant Total
9
Review Days
16

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Basic Information

Device Name
CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM
K Number
K953314
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Conceptus, Inc.
Date Received
July 12, 1995
Decision Date
July 28, 1995
Product Code
MOV
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MOV Catheters, Salpingography

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MOV), ordered by most recent decision date.

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Other Clearances by Conceptus, Inc.

K Number Device Name
K974028 STARGATE FALLOPOSCOPY CATHETER, TRIFURCATED IRRIGATION TUBING
K972210 RESECTOSCOPE SAFETY SHEATH
K962587 CONCEPTUS FALLOPIAN TUBE CATHETEIZATION WITH MICROENDOSCOPY SYSTEM
K954164 HYSTEROSCOPE
K932387 CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL
K932993 INTRAUTERINE CATHETER AND INTRODUCER
K933723 CONCEPTUS UTERINE CATHETER
K933981 CERVICAL CATHETER