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REDI-RELEASE ABSORBENT DRESSING

K904604 Class I Traditional
Decision Date
1991-01-07
Sponsor / Applicant
Fountain Pharmaceuticals, Inc.

Technical Specification

510(k) Submission ID K904604
Product Code KOZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4018
Decision Date 1991-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REDI-RELEASE ABSORBENT DRESSING received FDA 510(k) clearance under submission number K904604, sponsored by Fountain Pharmaceuticals, 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 1991-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code KOZ and 21 CFR 878.4018, within the General, Plastic Surgery review panel as a Class I device.