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FDA 510(k)

BACTEC PLUS AEROBIC/F AND ANAEROBIC/F MEDIA

K-Number: K921133 · 1992-04-22

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1992-04-22
Product CodeMDB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BACTEC PLUS AEROBIC/F AND ANAEROBIC/F MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1992-04-22 under 510(k) number K921133. The device is classified under product code MDB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACTEC PLUS AEROBIC/F AND ANAEROBIC/F MEDIA?

BACTEC PLUS AEROBIC/F AND ANAEROBIC/F MEDIA is a medical device that received FDA 510(k) clearance on 1992-04-22. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K921133.

When did BACTEC PLUS AEROBIC/F AND ANAEROBIC/F MEDIA receive FDA 510(k) clearance?

BACTEC PLUS AEROBIC/F AND ANAEROBIC/F MEDIA received FDA 510(k) clearance on 1992-04-22, under 510(k) number K921133.

Who is the listed applicant for BACTEC PLUS AEROBIC/F AND ANAEROBIC/F MEDIA?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BACTEC PLUS AEROBIC/F AND ANAEROBIC/F MEDIA?

The FDA product code for BACTEC PLUS AEROBIC/F AND ANAEROBIC/F MEDIA is MDB.

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Related Devices (Code: MDB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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