FDA 510(k)

NICKERSON'S MED. SELECTIVE CULTURE MEDIU

K-Number: K800754 · 1980-04-29

Decision Date1980-04-29

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

NICKERSON'S MED. SELECTIVE CULTURE MEDIU is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Pharmaceutical Corp.. It received FDA 510(k) clearance on 1980-04-29 under 510(k) number K800754. 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 NICKERSON'S MED. SELECTIVE CULTURE MEDIU?

NICKERSON'S MED. SELECTIVE CULTURE MEDIU is a medical device that received FDA 510(k) clearance on 1980-04-29. The listed applicant is Ortho Pharmaceutical Corp.. The 510(k) number is K800754.

When did NICKERSON'S MED. SELECTIVE CULTURE MEDIU receive FDA 510(k) clearance?

NICKERSON'S MED. SELECTIVE CULTURE MEDIU received FDA 510(k) clearance on 1980-04-29, under 510(k) number K800754.

Who is the listed applicant for NICKERSON'S MED. SELECTIVE CULTURE MEDIU?

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

What is the FDA product code for NICKERSON'S MED. SELECTIVE CULTURE MEDIU?

The FDA product code for NICKERSON'S MED. SELECTIVE CULTURE MEDIU 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.