Sunrise Sleep Disorder Diagnostic Aid— 510(k) DEN210015
UnknownSunrise
FDA 510(k) clearance DEN210015 for Sunrise Sleep Disorder Diagnostic Aid, Unknown on 2022-01-07. Applicant: Sunrise. Device class: 2.
Clearance details
- Applicant
- Sunrise
- Product code
- Code QRS
- Device class
- Class 2
- Regulation
- 21 CFR 868.2376
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Namur, BE
Recent devices under product code QRS
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