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FDA 510(k), K071560, PROVENT NASAL DILATOR, MODEL BR2
FDA 510(k), K071560, PROVENT NASAL DILATOR, MODEL BR2
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510(K) Number: K071560
Device Name: PROVENT NASAL DILATOR, MODEL BR2
Manufacturer: VENTUS MEDICAL, INC.
Device Classification Name: expiratory resistance valve, intranasal, for obstructive sleep apnea
Regulation Number: 872.5570
Classification Product Code: OHP
Date Received: 06/07/2007
Decision Date: 02/08/2008
Regulation Medical Specialty: Dental
Device Name: PROVENT NASAL DILATOR, MODEL BR2
Manufacturer: VENTUS MEDICAL, INC.
Device Classification Name: expiratory resistance valve, intranasal, for obstructive sleep apnea
Regulation Number: 872.5570
Classification Product Code: OHP
Date Received: 06/07/2007
Decision Date: 02/08/2008
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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