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DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSING

K991061 Class I Traditional
Decision Date
1999-06-28
Sponsor / Applicant
Dermaphylyx, Inc.

Technical Specification

510(k) Submission ID K991061
Product Code NAE
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4022
Decision Date 1999-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSING received FDA 510(k) clearance under submission number K991061, sponsored by Dermaphylyx, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1999-06-28.

Classification & Regulation

This clearance is catalogued under FDA product code NAE and 21 CFR 878.4022, within the General, Plastic Surgery review panel as a Class I device.