Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SORBSAN PLUS TOPICAL WOUND DRESSING

K-Number: K954230 · 1995-11-08

Decision Date1995-11-08
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SORBSAN PLUS TOPICAL WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Dow Hickam Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1995-11-08 under 510(k) number K954230. 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 SORBSAN PLUS TOPICAL WOUND DRESSING?

SORBSAN PLUS TOPICAL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1995-11-08. The listed applicant is Dow Hickam Pharmaceuticals, Inc.. The 510(k) number is K954230.

When did SORBSAN PLUS TOPICAL WOUND DRESSING receive FDA 510(k) clearance?

SORBSAN PLUS TOPICAL WOUND DRESSING received FDA 510(k) clearance on 1995-11-08, under 510(k) number K954230.

Who is the listed applicant for SORBSAN PLUS TOPICAL WOUND DRESSING?

The FDA 510(k) record lists Dow Hickam Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SORBSAN PLUS TOPICAL WOUND DRESSING?

The FDA product code for SORBSAN PLUS TOPICAL WOUND 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 Dow Hickam Pharmaceuticals, 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.

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.

↑