FDA 510(k)

HIPP BUFFER(NON-BARBITAL), P/N

K-Number: K801378 · 1980-07-14

Decision Date1980-07-14

Product CodeJJN

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

HIPP BUFFER(NON-BARBITAL), P/N is the device name listed in this FDA 510(k) record. The listed applicant is Gelman Sciences, Inc.. It received FDA 510(k) clearance on 1980-07-14 under 510(k) number K801378. The device is classified under product code JJN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIPP BUFFER(NON-BARBITAL), P/N?

HIPP BUFFER(NON-BARBITAL), P/N is a medical device that received FDA 510(k) clearance on 1980-07-14. The listed applicant is Gelman Sciences, Inc.. The 510(k) number is K801378.

When did HIPP BUFFER(NON-BARBITAL), P/N receive FDA 510(k) clearance?

HIPP BUFFER(NON-BARBITAL), P/N received FDA 510(k) clearance on 1980-07-14, under 510(k) number K801378.

Who is the listed applicant for HIPP BUFFER(NON-BARBITAL), P/N?

The FDA 510(k) record lists Gelman Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HIPP BUFFER(NON-BARBITAL), P/N?

The FDA product code for HIPP BUFFER(NON-BARBITAL), P/N is JJN.

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Other records listing Gelman Sciences, Inc. as applicant

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Related Devices (Code: JJN)

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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.