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..
Clearance details
- Applicant
- Neurovirtual USA, Inc.
- Product code
- Code MNR
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fort Lauderdale, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.