PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE— 510(k) K072372
Substantially EquivalentMego Afek
FDA 510(k) clearance K072372 for PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE, Substantially Equivalent on 2007-11-21. Applicant: Mego Afek.
Clearance details
- Applicant
- Mego Afek
- Product code
- Code JOW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kfar Saba, IL
Data sourced from openFDA. This site is unofficial and independent of the FDA.