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FDA 510(k), K013094, ORTHOSONIX ENERGEX
FDA 510(k), K013094, ORTHOSONIX ENERGEX
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510(K) Number: K013094
Device Name: ORTHOSONIX ENERGEX
Manufacturer: ORTHOSONIX, INC.
Device Classification Name: device, discharge, electrostatic (for pain relief)
Regulation Number: 890.5500
Classification Product Code: NHH
Date Received: 09/17/2001
Decision Date: 12/14/2001
Regulation Medical Specialty: Physical Medicine
Device Name: ORTHOSONIX ENERGEX
Manufacturer: ORTHOSONIX, INC.
Device Classification Name: device, discharge, electrostatic (for pain relief)
Regulation Number: 890.5500
Classification Product Code: NHH
Date Received: 09/17/2001
Decision Date: 12/14/2001
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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