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)

FLEXZAN WOUND DRESSING

K-Number: K954602 · 1995-11-02

Decision Date1995-11-02
Product CodeMGP
DecisionSubstantially Equivalent for Some Indications

Device Summary

FLEXZAN 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 1995-11-02 under 510(k) number K954602. The device is classified under product code MGP. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the FLEXZAN WOUND DRESSING?

FLEXZAN WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1995-11-02. The listed applicant is Dow Hickam Pharmaceuticals, Inc.. The 510(k) number is K954602.

When did FLEXZAN WOUND DRESSING receive FDA 510(k) clearance?

FLEXZAN WOUND DRESSING received FDA 510(k) clearance on 1995-11-02, under 510(k) number K954602.

Who is the listed applicant for FLEXZAN 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 FLEXZAN WOUND DRESSING?

The FDA product code for FLEXZAN WOUND DRESSING is MGP.

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: MGP)

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.

↑