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FDA 510(k), K041244, POLYGRAM NET BIOFEEDBACK APPLICATION
FDA 510(k), K041244, POLYGRAM NET BIOFEEDBACK APPLICATION
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510(K) Number: K041244
Device Name: POLYGRAM NET BIOFEEDBACK APPLICATION
Manufacturer: MEDTRONIC VASCULAR
Device Classification Name: Device, Biofeedback
Regulation Number: 882.5050
Classification Product Code: HCC
Date Received: 05/11/2004
Decision Date: 08/12/2004
Regulation Medical Specialty: Neurology
Device Name: POLYGRAM NET BIOFEEDBACK APPLICATION
Manufacturer: MEDTRONIC VASCULAR
Device Classification Name: Device, Biofeedback
Regulation Number: 882.5050
Classification Product Code: HCC
Date Received: 05/11/2004
Decision Date: 08/12/2004
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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