RAISIN PERSONAL MONITOR— 510(k) K093976
Substantially EquivalentProteus Biomedical, Inc.
FDA 510(k) clearance K093976 for RAISIN PERSONAL MONITOR, Substantially Equivalent on 2010-03-25. Applicant: Proteus Biomedical, Inc.. Device class: 2.
Clearance details
- Applicant
- Proteus Biomedical, Inc.
- Product code
- Code DXH
- Device class
- Class 2
- Regulation
- 21 CFR 870.2920
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Redwood City, CA, US
Recent devices under product code DXH
view allMore clearances from Proteus Biomedical, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.