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SINUS AC-POWERED MUSCLE STIMULATOR

K850453 Class II Traditional
Decision Date
1985-05-07
Sponsor / Applicant
Zimmer Elektromedizin GmbH

Technical Specification

510(k) Submission ID K850453
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1985-05-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SINUS AC-POWERED MUSCLE STIMULATOR received FDA 510(k) clearance under submission number K850453, sponsored by Zimmer Elektromedizin GmbH. 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 1985-05-07.

Classification & Regulation

This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.