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 |