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SKIN BARRIER FILM

K092712 Class I Traditional
Decision Date
2010-02-23
Sponsor / Applicant
Lodestar Products, Inc.

Technical Specification

510(k) Submission ID K092712
Product Code KMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5090
Decision Date 2010-02-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SKIN BARRIER FILM received FDA 510(k) clearance under submission number K092712, sponsored by Lodestar Products, Inc.. 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 2010-02-23.

Classification & Regulation

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