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SUPERSKIN

K972081 Class I Traditional
Decision Date
1997-12-17
Sponsor / Applicant
Medlogic Global Corp.

Technical Specification

510(k) Submission ID K972081
Product Code NEC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5090
Decision Date 1997-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUPERSKIN received FDA 510(k) clearance under submission number K972081, sponsored by Medlogic Global Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1997-12-17.

Classification & Regulation

This clearance is catalogued under FDA product code NEC and 21 CFR 880.5090, within the General Hospital review panel as a Class I device.