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FDA 510(k)

STOMAHESIVE PASTE PROTECTIVE SKIN BARR

K-Number: K803100 · 1981-01-08

ApplicantE. R. Squibb & Sons, Inc.
Decision Date1981-01-08
Product CodeEZR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STOMAHESIVE PASTE PROTECTIVE SKIN BARR is the device name listed in this FDA 510(k) record. The listed applicant is E. R. Squibb & Sons, Inc.. It received FDA 510(k) clearance on 1981-01-08 under 510(k) number K803100. The device is classified under product code EZR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOMAHESIVE PASTE PROTECTIVE SKIN BARR?

STOMAHESIVE PASTE PROTECTIVE SKIN BARR is a medical device that received FDA 510(k) clearance on 1981-01-08. The listed applicant is E. R. Squibb & Sons, Inc.. The 510(k) number is K803100.

When did STOMAHESIVE PASTE PROTECTIVE SKIN BARR receive FDA 510(k) clearance?

STOMAHESIVE PASTE PROTECTIVE SKIN BARR received FDA 510(k) clearance on 1981-01-08, under 510(k) number K803100.

Who is the listed applicant for STOMAHESIVE PASTE PROTECTIVE SKIN BARR?

The FDA 510(k) record lists E. R. Squibb & Sons, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STOMAHESIVE PASTE PROTECTIVE SKIN BARR?

The FDA product code for STOMAHESIVE PASTE PROTECTIVE SKIN BARR is EZR.

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Other records listing E. R. Squibb & Sons, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K821494RIA STAT 16K820616ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAYK820341CORTISOL-SQUIBB RADIOIMMUNOASSAY KITK820340T3 UPTAKE-SQUIBB DIAGNOSTIC KITK811240SUR-FIT LOOP OSTOMY O.R. SETK811239SUR-FIT DISPOSABLE CONVEX INSERT

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Related Devices (Code: EZR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K844341UNITED SKIN BARRIER PASTEHowmedica Corp.K791146COLO-TAPESuburban Ostomy Supply Co., Inc.K761340OSTOMY KARAYA GUM POWDERHowmedica Corp.K770230KARAYA GUM POWDERAtlantic SurgicalK761319KARAYA GUM PRODUCTS - PROCESS CHANGEHowmedica Corp.

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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