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THORACIC SUPPORT SYSTEM

K883214 Class I Traditional
Decision Date
1989-01-17
Sponsor / Applicant
Storer Medical Products

Technical Specification

510(k) Submission ID K883214
Product Code KMO
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5160
Decision Date 1989-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THORACIC SUPPORT SYSTEM received FDA 510(k) clearance under submission number K883214, sponsored by Storer Medical Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1989-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code KMO and 21 CFR 880.5160, within the General Hospital review panel as a Class I device.