MASTERSCREEN IOS— 510(k) K101873
Substantially EquivalentCarefusion Germany 234 GmbH
FDA 510(k) clearance K101873 for MASTERSCREEN IOS, Substantially Equivalent on 2011-02-10. Applicant: Carefusion Germany 234 GmbH. Device class: 2.
Clearance details
- Applicant
- Carefusion Germany 234 GmbH
- Product code
- Code BZG
- Device class
- Class 2
- Regulation
- 21 CFR 868.1840
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hoechberg, DE
Recent devices under product code BZG
view allMore clearances from Carefusion Germany 234 GmbH
view allData sourced from openFDA. This site is unofficial and independent of the FDA.