Maxxi Snore Sensor— 510(k) K191095
Substantially EquivalentNeurovirtual USA, Inc.
FDA 510(k) clearance K191095 for Maxxi Snore Sensor, Substantially Equivalent on 2020-01-16. 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
- Fort Lauderdale, FL, US
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