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FDA 510(k), K170825, SnoreRx
FDA 510(k), K170825, SnoreRx
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510(K) Number: K170825
Device Name: SnoreRx
Manufacturer: Apnea Sciences Corporation
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 03/20/2017
Decision Date: 08/18/2017
Regulation Medical Specialty: Dental
Device Name: SnoreRx
Manufacturer: Apnea Sciences Corporation
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 03/20/2017
Decision Date: 08/18/2017
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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