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FDA 510(k)

3M NO STING BARRIER FILM

K-Number: K955103 · 1996-02-05

Decision Date1996-02-05
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

3M NO STING BARRIER FILM is the device name listed in this FDA 510(k) record. The listed applicant is 3M Medical Products Group. It received FDA 510(k) clearance on 1996-02-05 under 510(k) number K955103. 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 NO STING BARRIER FILM?

3M NO STING BARRIER FILM is a medical device that received FDA 510(k) clearance on 1996-02-05. The listed applicant is 3M Medical Products Group. The 510(k) number is K955103.

When did 3M NO STING BARRIER FILM receive FDA 510(k) clearance?

3M NO STING BARRIER FILM received FDA 510(k) clearance on 1996-02-05, under 510(k) number K955103.

Who is the listed applicant for 3M NO STING BARRIER FILM?

The FDA 510(k) record lists 3M Medical Products Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M NO STING BARRIER FILM?

The FDA product code for 3M NO STING BARRIER FILM is KMF.

Related Clinical Trials

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.

Other records listing 3M Medical Products Group 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.

View all 12 devices →

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.

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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