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FDA 510(k)

ALLKARE BARRIER WIPE

K-Number: K925004 · 1994-01-12

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1994-01-12
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALLKARE BARRIER WIPE is the device name listed in this FDA 510(k) record. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. It received FDA 510(k) clearance on 1994-01-12 under 510(k) number K925004. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLKARE BARRIER WIPE?

ALLKARE BARRIER WIPE is a medical device that received FDA 510(k) clearance on 1994-01-12. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K925004.

When did ALLKARE BARRIER WIPE receive FDA 510(k) clearance?

ALLKARE BARRIER WIPE received FDA 510(k) clearance on 1994-01-12, under 510(k) number K925004.

Who is the listed applicant for ALLKARE BARRIER WIPE?

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

What is the FDA product code for ALLKARE BARRIER WIPE?

The FDA product code for ALLKARE BARRIER WIPE is KMF.

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Other records listing Convatec, A Division of E.R. Squibb & Sons 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.

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Related Devices (Code: KMF)

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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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