CEFAR REHAB 2 AND REHAB 2 PRO— 510(k) K030403
Substantially EquivalentCefar Medical AB
FDA 510(k) clearance K030403 for CEFAR REHAB 2 AND REHAB 2 PRO, Substantially Equivalent on 2003-07-17. Applicant: Cefar Medical AB.
Clearance details
- Applicant
- Cefar Medical AB
- Product code
- Code IPF
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis,, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.