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. Device class: 2.
Clearance details
- Applicant
- Cefar Medical AB
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis,, MN, US
Recent devices under product code IPF
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