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PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE

K000655 Class II Traditional
Decision Date
2001-03-26
Sponsor / Applicant
Ahava Stein

Technical Specification

510(k) Submission ID K000655
Product Code IRP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5650
Decision Date 2001-03-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE received FDA 510(k) clearance under submission number K000655, sponsored by Ahava Stein. 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 2001-03-26.

Classification & Regulation

This clearance is catalogued under FDA product code IRP and 21 CFR 890.5650, within the Physical Medicine review panel as a Class II device.