meddevicedb.com FDA Device Reference

MULTIPLE

K853297 Class I Traditional
Decision Date
1985-11-05
Sponsor / Applicant
Sun Air, Inc.

Technical Specification

510(k) Submission ID K853297
Product Code ISA
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5660
Decision Date 1985-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTIPLE received FDA 510(k) clearance under submission number K853297, sponsored by Sun Air, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1985-11-05.

Classification & Regulation

This clearance is catalogued under FDA product code ISA and 21 CFR 890.5660, within the Physical Medicine review panel as a Class I device.