PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 80); PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 50)— 510(k) K102404
Substantially EquivalentVentus Medical, Inc.
FDA 510(k) clearance K102404 for PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 80); PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 50), Substantially Equivalent on 2010-12-02. Applicant: Ventus Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Ventus Medical, Inc.
- Product code
- Code OHP
- Device class
- Class 2
- Regulation
- 21 CFR 872.5570
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Belmont, CA, US
Recent devices under product code OHP
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