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 |