LYMPHA PRESS
Sleeve, Limb, Compressible
MEGO AFEK
The following data is part of a premarket notification filed by Mego Afek with the FDA for Lympha Press.
Pre-market Notification Details
| Device ID | K810338 |
| 510k Number | K810338 |
| Device Name: | LYMPHA PRESS |
| Classification | Sleeve, Limb, Compressible |
| Applicant | MEGO AFEK 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | JOW |
| CFR Regulation Number | 870.5800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-02-09 |
| Decision Date | 1981-10-20 |
Trademark Results [LYMPHA PRESS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LYMPHA PRESS 98565220 not registered Live/Pending |
Mego Afek AC Ltd. 2024-05-23 |
 LYMPHA PRESS 73293385 1225852 Live/Registered |
MEGO-AFEK INDUSTRIAL MEASURING INSTRUMENTS 1981-01-16 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.