FDA 510(k)

SELECTIVE CHARCOAL YEAST EXTRACT AGAR

K-Number: K802758 · 1980-12-31

Decision Date1980-12-31

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SELECTIVE 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 1980-12-31 under 510(k) number K802758. 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 SELECTIVE CHARCOAL YEAST EXTRACT AGAR?

SELECTIVE CHARCOAL YEAST EXTRACT AGAR is a medical device that received FDA 510(k) clearance on 1980-12-31. The listed applicant is Remel Co.. The 510(k) number is K802758.

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

SELECTIVE CHARCOAL YEAST EXTRACT AGAR received FDA 510(k) clearance on 1980-12-31, under 510(k) number K802758.

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

The FDA product code for SELECTIVE CHARCOAL YEAST EXTRACT 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.