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FDA 510(k)

HOLLISTER KARAYA PASTE

K-Number: K791525 · 1979-10-26

ApplicantHollister, Inc.
Decision Date1979-10-26
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOLLISTER KARAYA PASTE is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1979-10-26 under 510(k) number K791525. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOLLISTER KARAYA PASTE?

HOLLISTER KARAYA PASTE is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is Hollister, Inc.. The 510(k) number is K791525.

When did HOLLISTER KARAYA PASTE receive FDA 510(k) clearance?

HOLLISTER KARAYA PASTE received FDA 510(k) clearance on 1979-10-26, under 510(k) number K791525.

Who is the listed applicant for HOLLISTER KARAYA PASTE?

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

What is the FDA product code for HOLLISTER KARAYA PASTE?

The FDA product code for HOLLISTER KARAYA PASTE is EXB.

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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.

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