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)

DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING

K-Number: K990875 · 1999-05-27

Decision Date1999-05-27
Product CodeMGP
DecisionSubstantially Equivalent for Some Indications

Device Summary

DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Dermaphylyx, Inc.. It received FDA 510(k) clearance on 1999-05-27 under 510(k) number K990875. The device is classified under product code MGP. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING?

DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1999-05-27. The listed applicant is Dermaphylyx, Inc.. The 510(k) number is K990875.

When did DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING receive FDA 510(k) clearance?

DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING received FDA 510(k) clearance on 1999-05-27, under 510(k) number K990875.

Who is the listed applicant for DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING?

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

What is the FDA product code for DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING?

The FDA product code for DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM 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 Dermaphylyx, 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 9 devices →

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.

↑