meddevicedb.com FDA Device Reference

SAF SINGLE-USE AEROSOL FILTER

K811203 Class I Traditional
Decision Date
1981-05-21
Sponsor / Applicant
Sorensen Research

Technical Specification

510(k) Submission ID K811203
Product Code GCY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4680
Decision Date 1981-05-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SAF SINGLE-USE AEROSOL FILTER received FDA 510(k) clearance under submission number K811203, sponsored by Sorensen Research. 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 1981-05-21.

Classification & Regulation

This clearance is catalogued under FDA product code GCY and 21 CFR 878.4680, within the General, Plastic Surgery review panel as a Class I device.