Maxxi Rip Sensor— 510(k) K171304
Substantially EquivalentNeurovirtual USA, Inc.
FDA 510(k) clearance K171304 for Maxxi Rip Sensor, Substantially Equivalent on 2019-06-24. Applicant: Neurovirtual USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Neurovirtual USA, 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
- Doral, FL, US
Recent devices under product code MNR
view allMore clearances from Neurovirtual USA, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.