Ventus Medical, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Advertisement
Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K120665 | INVENT SNORING DEVICE | LWF | 2012-06-12 | View |
| 510(k) | K102404 | PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 80); PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 50) | OHP | 2010-12-02 | View |
| 510(k) | K090398 | PROVENT PROFESSIONAL SLEEP APNEA THERAPY | OHP | 2009-04-03 | View |
| 510(k) | K080983 | PROVENT NASAL CANNULA | MNR | 2008-08-07 | View |
| 510(k) | K071560 | PROVENT NASAL DILATOR, MODEL BR2 | OHP | 2008-02-08 | View |
No matching devices.
Advertisement