FDA 510(k)

SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA

K-Number: K923892 · 1993-06-21

Decision Date1993-06-21

Product CodeJSO

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Smith River Biologicals. It received FDA 510(k) clearance on 1993-06-21 under 510(k) number K923892. The device is classified under product code JSO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA?

SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA is a medical device that received FDA 510(k) clearance on 1993-06-21. The listed applicant is Smith River Biologicals. The 510(k) number is K923892.

When did SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA receive FDA 510(k) clearance?

SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA received FDA 510(k) clearance on 1993-06-21, under 510(k) number K923892.

Who is the listed applicant for SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA?

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

What is the FDA product code for SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA?

The FDA product code for SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA is JSO.

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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.