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PULSARII, HIGH VOLT. GALVANIC MUSC. STIM

K810064 Class II Traditional
Decision Date
1981-01-26
Sponsor / Applicant
Bomed Medical Mfr., Ltd.

Technical Specification

510(k) Submission ID K810064
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1981-01-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PULSARII, HIGH VOLT. GALVANIC MUSC. STIM received FDA 510(k) clearance under submission number K810064, sponsored by Bomed Medical Mfr., Ltd.. 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 1981-01-26.

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.