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FDA 510(k)

GLASION VARNISH

K-Number: K915376 · 1992-01-22

ApplicantSci-Pharm Scientific Pharmaceutical, Inc.
Decision Date1992-01-22
Product CodeFMC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GLASION VARNISH is the device name listed in this FDA 510(k) record. The listed applicant is Sci-Pharm Scientific Pharmaceutical, Inc.. It received FDA 510(k) clearance on 1992-01-22 under 510(k) number K915376. The device is classified under product code FMC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLASION VARNISH?

GLASION VARNISH is a medical device that received FDA 510(k) clearance on 1992-01-22. The listed applicant is Sci-Pharm Scientific Pharmaceutical, Inc.. The 510(k) number is K915376.

When did GLASION VARNISH receive FDA 510(k) clearance?

GLASION VARNISH received FDA 510(k) clearance on 1992-01-22, under 510(k) number K915376.

Who is the listed applicant for GLASION VARNISH?

The FDA 510(k) record lists Sci-Pharm Scientific Pharmaceutical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GLASION VARNISH?

The FDA product code for GLASION VARNISH is FMC.

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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.

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