meddevicedb.com FDA Device Reference

MASK, SURGEONS

K780607 Class II Traditional
Decision Date
1978-06-22
Sponsor / Applicant
Abco Dealers, Inc.

Technical Specification

510(k) Submission ID K780607
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1978-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MASK, SURGEONS received FDA 510(k) clearance under submission number K780607, sponsored by Abco Dealers, Inc.. 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 1978-06-22.

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.