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FDA 510(k)

MESALT STERILE DRESSING

K-Number: K934839 · 1993-12-22

Decision Date1993-12-22
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MESALT STERILE 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 1993-12-22 under 510(k) number K934839. 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 MESALT STERILE DRESSING?

MESALT STERILE DRESSING is a medical device that received FDA 510(k) clearance on 1993-12-22. The listed applicant is Richard Hamer Assoc., Inc.. The 510(k) number is K934839.

When did MESALT STERILE DRESSING receive FDA 510(k) clearance?

MESALT STERILE DRESSING received FDA 510(k) clearance on 1993-12-22, under 510(k) number K934839.

Who is the listed applicant for MESALT STERILE 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 MESALT STERILE DRESSING?

The FDA product code for MESALT STERILE 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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