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.. Device class: 2.
Clearance details
- Applicant
- Mego Afek AC , Ltd.
- Product code
- Code JOW
- Device class
- Class 2
- Regulation
- 21 CFR 870.5800
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kfar Saba, IL
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