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FDA 510(k), K160239, TAP 3, TAP 1
FDA 510(k), K160239, TAP 3, TAP 1
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510(K) Number: K160239
Device Name: TAP 3, TAP 1
Manufacturer: Airway Management, Inc.
Device Classification Name: sleep appliances with patient monitoring
Regulation Number: 872.5570
Classification Product Code: PLC
Date Received: 02/01/2016
Decision Date: 08/10/2016
Regulation Medical Specialty: Dental
Device Name: TAP 3, TAP 1
Manufacturer: Airway Management, Inc.
Device Classification Name: sleep appliances with patient monitoring
Regulation Number: 872.5570
Classification Product Code: PLC
Date Received: 02/01/2016
Decision Date: 08/10/2016
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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