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: MDB FDA class 1

System, Blood Culturing

Microbiology

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The blood culturing system is a microbiology laboratory device used to incubate and monitor blood samples for the presence and growth of bacteria or fungi, supporting the diagnosis of bacteremia and septicemia. It is classified as FDA Class I under 21 CFR 866.2560 within the Microbiology specialty, subject only to general controls. The product code is MDB and the device is not GMP-exempt. It is not implanted and does not sustain life.

510(k) Clearances

50+ matches
K Number
Device Name
BD BACTEC™ Plus Aerobic/F Culture Vials
BD BACTEC™ Myco/F Lytic Culture Vials
BACT/ALERT MP Reagent System
BacT/ALERT FA Plus; BacT/ALERT PF Plus
BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial
BacT/ALERT VIRTUO Microbial Detection System, BacT/ALERT VIRTUO, VIRTUO
BD BACTEC Standard/10 Aerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial
BD BACTEC Standard Anaerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial
BD BACTEC Peds Plus/F Culture Vials (plastic)
BD BACTEC PLUS ANAEROBIC/F (PLASTIC)
BACTEC Lytic/10 Anaerobic/F Culture Vials (plastic)
BACT/ALERT FN PLUS CULTURE BOTTLE
BACT/ALERT PF PLUS CULTURE BOTTLE
BACT/ALERT FA PLUS CULTURE BOTTLE
BD BACTEC Plus PRIME Aerobic/F Culture Vials
BD BACTEC Plus Aerobic/F Culture Vials (plastic)
BD BACTEC Plus Aerobic/F Culture Vials
VERSATREK
BACT/ALERT MP CULTURE BOTTLES (PLASTIC)
BACT/ALERT SN CULTURE BOTTLE
BACT/ALERT PF CULTURE BOTTLE
BACT/ALERT FN CULTURE BOTTLE
BACT/ALERT SA CULTURE BOTTLE
BACT/ALERT FA CULTURE BOTTLE
BACT/ALERT MB CULTURE BOTTLE
BACT/ALERT SV
BACT/ALERT SA
BACT/ALERT SN
BACT/ALERT MP PROCESS BOTTLE
BACT/ALERT FN
BACT/ALERT PF
BACTALERT FA
MB/BACT BLOOD CULTURE BOTTLE
MB/BACT BLOOD CULTURE BOTTLE
BACT/ALERT 3D MICROBIAL DETECTION SYSTEM
BACTEC MGIT 960 SYSTEM
BACTEC MYCO/F LYTIC CULTURE VIALS
BACTEC MYCO/F LYTIC CULTURE VIALS
BACT/ALERT FAN CULTURE BOTTLES
BACT/ALERT CULTURE BOTTLES
BACTEC MYCO/F-SPUTA CULTURE VIALS
MODIFICATION OF EST CULTURE SYSTEM II - MYCO
BBL MGIT PRODUCTS
BACTEC 9050 SYSTEM
MB/BACT MYCROBACTERIA DETECTION SYSTEM
BACTEC(R) 9000TB SYSTEM
BACTEC STANDARD/10 AEROBIC/F CULTURE VIALS
BACTEC PEDS PLUS/F CULTURE VIALS
BACTEC LYTIC/10 ANAEROBIC/F CULTURE VIALS
BACTEC CULTURE VIALS, LYTIC, ANAEROBIC

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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