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FDA 510(k), K103031, BMR FACE
FDA 510(k), K103031, BMR FACE
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510(K) Number: K103031
Device Name: BMR FACE
Manufacturer: ANNE-MARIE KEENAN
Device Classification Name: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation Number: NFO
Classification Product Code: 10/12/2010
Date Received: 11/10/2011
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: BMR FACE
Manufacturer: ANNE-MARIE KEENAN
Device Classification Name: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation Number: NFO
Classification Product Code: 10/12/2010
Date Received: 11/10/2011
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
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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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