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SAFESKIN SUPRA

K953015 Class I Traditional
Decision Date
1995-08-28
Sponsor / Applicant
Safeskin Corp.

Technical Specification

510(k) Submission ID K953015
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1995-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SAFESKIN SUPRA received FDA 510(k) clearance under submission number K953015, sponsored by Safeskin Corp.. 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 1995-08-28.

Classification & Regulation

This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.