CEFAR MEDICAL AB CEFAR PRIMO— 510(k) K020803
Substantially EquivalentCefar Medical AB
FDA 510(k) clearance K020803 for CEFAR MEDICAL AB CEFAR PRIMO, Substantially Equivalent on 2002-06-10. Applicant: Cefar Medical AB. Device class: 2.
Clearance details
- Applicant
- Cefar Medical AB
- Product code
- Code GZJ
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis,, MN, US
Recent devices under product code GZJ
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