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ESCAPE CONTROL MODULE

K021995 Class II Traditional
Decision Date
2002-08-01
Sponsor / Applicant
Specialty Drives Technologies, Inc.

Technical Specification

510(k) Submission ID K021995
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2002-08-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ESCAPE CONTROL MODULE received FDA 510(k) clearance under submission number K021995, sponsored by Specialty Drives Technologies, 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 2002-08-01.

Classification & Regulation

This clearance is catalogued under FDA product code ITI and 21 CFR 890.3860, within the Physical Medicine review panel as a Class II device.