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FDA 510(k)

3M INCONTINENCE BARRIER FILM, PRODUCT SERIES 336X

K-Number: K930468 · 1993-08-06

Applicant3M Health Care, Ltd.
Decision Date1993-08-06
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

3M INCONTINENCE BARRIER FILM, PRODUCT SERIES 336X is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Ltd.. It received FDA 510(k) clearance on 1993-08-06 under 510(k) number K930468. 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 3M INCONTINENCE BARRIER FILM, PRODUCT SERIES 336X?

3M INCONTINENCE BARRIER FILM, PRODUCT SERIES 336X is a medical device that received FDA 510(k) clearance on 1993-08-06. The listed applicant is 3M Health Care, Ltd.. The 510(k) number is K930468.

When did 3M INCONTINENCE BARRIER FILM, PRODUCT SERIES 336X receive FDA 510(k) clearance?

3M INCONTINENCE BARRIER FILM, PRODUCT SERIES 336X received FDA 510(k) clearance on 1993-08-06, under 510(k) number K930468.

Who is the listed applicant for 3M INCONTINENCE BARRIER FILM, PRODUCT SERIES 336X?

The FDA 510(k) record lists 3M Health Care, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M INCONTINENCE BARRIER FILM, PRODUCT SERIES 336X?

The FDA product code for 3M INCONTINENCE BARRIER FILM, PRODUCT SERIES 336X is KMF.

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Other records listing 3M Health Care, Ltd. as applicant

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Related Devices (Code: KMF)

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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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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