PROVENT NASAL CANNULA— 510(k) K080983
Substantially EquivalentVentus Medical, Inc.
FDA 510(k) clearance K080983 for PROVENT NASAL CANNULA, Substantially Equivalent on 2008-08-07. Applicant: Ventus Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Ventus Medical, Inc.
- Product code
- Code MNR
- Device class
- Class 2
- Regulation
- 21 CFR 868.2375
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Belmont, CA, US
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