The following data is part of a premarket notification filed by Medi Usa, Lp with the FDA for Medi Strumpf.
| Device ID | K941926 |
| 510k Number | K941926 |
| Device Name: | MEDI STRUMPF |
| Classification | Stocking, Medical Support (to Prevent Pooling Of Blood In Legs) |
| Applicant | MEDI USA, LP 76 W. SEEGERS RD. Arlington Heights, IL 60005 |
| Contact | D. Bruce Guynn |
| Correspondent | D. Bruce Guynn MEDI USA, LP 76 W. SEEGERS RD. Arlington Heights, IL 60005 |
| Product Code | DWL |
| CFR Regulation Number | 880.5780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-04-20 |
| Decision Date | 1994-06-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEDI STRUMPF 74588752 1975907 Dead/Cancelled |
WEIHERMULLER & VOIGTMANN GMBH & CO KG 1994-10-21 |