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MASK, SURGICAL, DISP

K770513 Class II Traditional
Decision Date
1977-04-29
Sponsor / Applicant
Acme Automatic Disposable

Technical Specification

510(k) Submission ID K770513
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1977-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MASK, SURGICAL, DISP received FDA 510(k) clearance under submission number K770513, sponsored by Acme Automatic Disposable. 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 1977-04-29.

Classification & Regulation

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