QDC-PRO, AND NOX-RIP— 510(k) K124062
Substantially EquivalentNox Medical
FDA 510(k) clearance K124062 for QDC-PRO, AND NOX-RIP, Substantially Equivalent on 2013-07-10. Applicant: Nox Medical. Device class: 2.
Clearance details
- Applicant
- Nox Medical
- 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
- Reykjavik, IS
Recent devices under product code MNR
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