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PRIZM MEDICAL, INC. MICRO-Z STIMULATION SYSTEM

K024181 Class II Traditional
Decision Date
2003-06-26
Sponsor / Applicant
Prizm Medical, Inc.

Technical Specification

510(k) Submission ID K024181
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2003-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRIZM MEDICAL, INC. MICRO-Z STIMULATION SYSTEM received FDA 510(k) clearance under submission number K024181, sponsored by Prizm Medical, 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 2003-06-26.

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.