LYMPHA PRESS 201MAX, MODEL 201MAX— 510(k) K100677
Substantially EquivalentMego Afek AC , Ltd.
FDA 510(k) clearance K100677 for LYMPHA PRESS 201MAX, MODEL 201MAX, Substantially Equivalent on 2010-05-20. Applicant: Mego Afek AC , Ltd..
Clearance details
- Applicant
- Mego Afek AC , Ltd.
- 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.