FDA 510(k)

BUFFERED CYE AGAR DEEP W/SUPPLEMENTS

K-Number: K840890 · 1984-03-23

Decision Date1984-03-23

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

BUFFERED CYE AGAR DEEP W/SUPPLEMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1984-03-23 under 510(k) number K840890. 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 CYE AGAR DEEP W/SUPPLEMENTS?

BUFFERED CYE AGAR DEEP W/SUPPLEMENTS is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Remel Co.. The 510(k) number is K840890.

When did BUFFERED CYE AGAR DEEP W/SUPPLEMENTS receive FDA 510(k) clearance?

BUFFERED CYE AGAR DEEP W/SUPPLEMENTS received FDA 510(k) clearance on 1984-03-23, under 510(k) number K840890.

Who is the listed applicant for BUFFERED CYE AGAR DEEP W/SUPPLEMENTS?

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 CYE AGAR DEEP W/SUPPLEMENTS?

The FDA product code for BUFFERED CYE AGAR DEEP W/SUPPLEMENTS 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.