meddevicedb.com FDA Device Reference

INFINITECH BREATH EZ

K935441 Class I Traditional
Decision Date
1994-02-07
Sponsor / Applicant
Infinitech, Inc.

Technical Specification

510(k) Submission ID K935441
Product Code BWN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4950
Decision Date 1994-02-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INFINITECH BREATH EZ received FDA 510(k) clearance under submission number K935441, sponsored by Infinitech, 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 1994-02-07.

Classification & Regulation

This clearance is catalogued under FDA product code BWN and 21 CFR 878.4950, within the General, Plastic Surgery review panel as a Class I device.