APNEALINK, MODEL 22302— 510(k) K061405
Substantially EquivalentResmed Germany, Inc.
FDA 510(k) clearance K061405 for APNEALINK, MODEL 22302, Substantially Equivalent on 2006-07-25. Applicant: Resmed Germany, Inc.. Device class: 2.
Clearance details
- Applicant
- Resmed Germany, 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
- Poway, CA, US
Recent devices under product code MNR
view allMore clearances from Resmed Germany, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.