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FDA 510(k), K030714, PEAK MOTUS
FDA 510(k), K030714, PEAK MOTUS
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510(K) Number: K030714
Device Name: PEAK MOTUS
Manufacturer: PEAK PERFORMANCE TECHNOLOGIES, INC
Device Classification Name: interactive rehabilitation exercise devices
Regulation Number: 890.5360
Classification Product Code: LXJ
Date Received: 03/06/2003
Decision Date: 05/16/2003
Regulation Medical Specialty: Physical Medicine
Device Name: PEAK MOTUS
Manufacturer: PEAK PERFORMANCE TECHNOLOGIES, INC
Device Classification Name: interactive rehabilitation exercise devices
Regulation Number: 890.5360
Classification Product Code: LXJ
Date Received: 03/06/2003
Decision Date: 05/16/2003
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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