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FDA 510(k)

ANAEROBIC PEA BLOOD AGAR

K-Number: K871090 · 1987-04-03

ApplicantbioMerieux, Inc.
Decision Date1987-04-03
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANAEROBIC PEA BLOOD AGAR is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 1987-04-03 under 510(k) number K871090. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANAEROBIC PEA BLOOD AGAR?

ANAEROBIC PEA BLOOD AGAR is a medical device that received FDA 510(k) clearance on 1987-04-03. The listed applicant is bioMerieux, Inc.. The 510(k) number is K871090.

When did ANAEROBIC PEA BLOOD AGAR receive FDA 510(k) clearance?

ANAEROBIC PEA BLOOD AGAR received FDA 510(k) clearance on 1987-04-03, under 510(k) number K871090.

Who is the listed applicant for ANAEROBIC PEA BLOOD AGAR?

The FDA 510(k) record lists bioMerieux, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANAEROBIC PEA BLOOD AGAR?

The FDA product code for ANAEROBIC PEA BLOOD AGAR is JSJ.

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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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