SomnoMetry— 510(k) K221179
Substantially EquivalentNeumetry Medical, Inc.
FDA 510(k) clearance K221179 for SomnoMetry, Substantially Equivalent on 2022-09-21. Applicant: Neumetry Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Neumetry Medical, Inc.
- Product code
- Code OLZ
- Device class
- Class 2
- Regulation
- 21 CFR 882.1400
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fremont, CA, US
Recent devices under product code OLZ
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