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FDA 510(k), K954530, THE SILENCER
FDA 510(k), K954530, THE SILENCER
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510(K) Number: K954530
Device Name: THE SILENCER
Manufacturer: SILENT KNIGHTS VENTURES, INC.
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 09/29/1995
Decision Date: 10/30/1995
Regulation Medical Specialty: Dental
Device Name: THE SILENCER
Manufacturer: SILENT KNIGHTS VENTURES, INC.
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 09/29/1995
Decision Date: 10/30/1995
Regulation Medical Specialty: Dental
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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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