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FDA 510(k)

SALMONELLA FLAGELLAR A ANTIGEN & B

K-Number: K801693 · 1980-08-27

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1980-08-27
Product CodeGNC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SALMONELLA FLAGELLAR A ANTIGEN & B 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 1980-08-27 under 510(k) number K801693. The device is classified under product code GNC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALMONELLA FLAGELLAR A ANTIGEN & B?

SALMONELLA FLAGELLAR A ANTIGEN & B is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K801693.

When did SALMONELLA FLAGELLAR A ANTIGEN & B receive FDA 510(k) clearance?

SALMONELLA FLAGELLAR A ANTIGEN & B received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801693.

Who is the listed applicant for SALMONELLA FLAGELLAR A ANTIGEN & B?

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 SALMONELLA FLAGELLAR A ANTIGEN & B?

The FDA product code for SALMONELLA FLAGELLAR A ANTIGEN & B is GNC.

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Related Devices (Code: GNC)

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.

K972388VISTA ANTIGEN SALMONELLA O GROUP CLee Laboratories, Inc.K972395VISTA ANTIGEN SALMONELLA O GROUP DLee Laboratories, Inc.K972389VISTA ANTIGEN SALMONELLA H DLee Laboratories, Inc.K972387VISTA ANTIGEN SALMONELLA O GROUP ALee Laboratories, Inc.K972386VISTA ANTIGEN SALMONELLA O GROUP BLee Laboratories, Inc.K972391VISTA ANTIGEN SALMONELLA H BLee Laboratories, Inc.

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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