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FDA 510(k)

HOLLISTER SKIN BARRIER A

K-Number: K810709 · 1981-04-07

ApplicantHollister, Inc.
Decision Date1981-04-07
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOLLISTER SKIN BARRIER A is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1981-04-07 under 510(k) number K810709. 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 SKIN BARRIER A?

HOLLISTER SKIN BARRIER A is a medical device that received FDA 510(k) clearance on 1981-04-07. The listed applicant is Hollister, Inc.. The 510(k) number is K810709.

When did HOLLISTER SKIN BARRIER A receive FDA 510(k) clearance?

HOLLISTER SKIN BARRIER A received FDA 510(k) clearance on 1981-04-07, under 510(k) number K810709.

Who is the listed applicant for HOLLISTER SKIN BARRIER A?

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 SKIN BARRIER A?

The FDA product code for HOLLISTER SKIN BARRIER A 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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