SOMNOSCREEN— 510(k) K060708
Substantially EquivalentSomnomedics GmbH & Co. KG
FDA 510(k) clearance K060708 for SOMNOSCREEN, Substantially Equivalent on 2007-01-24. Applicant: Somnomedics GmbH & Co. KG. Device class: 2.
Clearance details
- Applicant
- Somnomedics GmbH & Co. KG
- 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
- Washington, DC, US
Recent devices under product code MNR
view allData sourced from openFDA. This site is unofficial and independent of the FDA.