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FLOTATION UNIT, CHAIR

K760613 Class I Traditional
Decision Date
1976-10-14
Sponsor / Applicant
Medpro, Inc.

Technical Specification

510(k) Submission ID K760613
Product Code KIC
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3175
Decision Date 1976-10-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLOTATION UNIT, CHAIR received FDA 510(k) clearance under submission number K760613, sponsored by Medpro, 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 1976-10-14.

Classification & Regulation

This clearance is catalogued under FDA product code KIC and 21 CFR 890.3175, within the Physical Medicine review panel as a Class I device.