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FDA 510(k)

COMFEEL PLUS CONTOUR DRESSING

K-Number: K951327 · 1995-04-28

Decision Date1995-04-28
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COMFEEL PLUS CONTOUR DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Richard Hamer Assoc., Inc.. It received FDA 510(k) clearance on 1995-04-28 under 510(k) number K951327. 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 COMFEEL PLUS CONTOUR DRESSING?

COMFEEL PLUS CONTOUR DRESSING is a medical device that received FDA 510(k) clearance on 1995-04-28. The listed applicant is Richard Hamer Assoc., Inc.. The 510(k) number is K951327.

When did COMFEEL PLUS CONTOUR DRESSING receive FDA 510(k) clearance?

COMFEEL PLUS CONTOUR DRESSING received FDA 510(k) clearance on 1995-04-28, under 510(k) number K951327.

Who is the listed applicant for COMFEEL PLUS CONTOUR DRESSING?

The FDA 510(k) record lists Richard Hamer Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMFEEL PLUS CONTOUR DRESSING?

The FDA product code for COMFEEL PLUS CONTOUR DRESSING 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 Richard Hamer Assoc., 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.

View all 8 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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