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LAC-MAC LIMITED INNERBLOC O.R. GOWN

K030536 Class II Traditional
Decision Date
2003-05-06
Sponsor / Applicant
Lac Mac, Ltd.

Technical Specification

510(k) Submission ID K030536
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2003-05-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LAC-MAC LIMITED INNERBLOC O.R. GOWN received FDA 510(k) clearance under submission number K030536, sponsored by Lac Mac, Ltd.. 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 2003-05-06.

Classification & Regulation

This clearance is catalogued under FDA product code FYA and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.