FDA 510(k)

BUFFERED CHARCOAL YEAST EXTRACT AGAR

K-Number: K802757 · 1981-01-08

Decision Date1981-01-08

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

BUFFERED CHARCOAL YEAST EXTRACT AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1981-01-08 under 510(k) number K802757. 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 BUFFERED CHARCOAL YEAST EXTRACT AGAR?

BUFFERED CHARCOAL YEAST EXTRACT AGAR is a medical device that received FDA 510(k) clearance on 1981-01-08. The listed applicant is Remel Co.. The 510(k) number is K802757.

When did BUFFERED CHARCOAL YEAST EXTRACT AGAR receive FDA 510(k) clearance?

BUFFERED CHARCOAL YEAST EXTRACT AGAR received FDA 510(k) clearance on 1981-01-08, under 510(k) number K802757.

Who is the listed applicant for BUFFERED CHARCOAL YEAST EXTRACT AGAR?

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

What is the FDA product code for BUFFERED CHARCOAL YEAST EXTRACT AGAR?

The FDA product code for BUFFERED CHARCOAL YEAST EXTRACT AGAR is JSJ.

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Official Source

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