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FDA 510(k), K972723, BIO TROL
FDA 510(k), K972723, BIO TROL
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510(K) Number: K972723
Device Name: BIO TROL
Manufacturer: MINDMEDIA LABS, INC.
Device Classification Name: device, biofeedback
Regulation Number: 882.5050
Classification Product Code: HCC
Date Received: 07/21/1997
Decision Date: 10/02/1997
Regulation Medical Specialty: Neurology
Device Name: BIO TROL
Manufacturer: MINDMEDIA LABS, INC.
Device Classification Name: device, biofeedback
Regulation Number: 882.5050
Classification Product Code: HCC
Date Received: 07/21/1997
Decision Date: 10/02/1997
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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