The following data is part of a premarket notification filed by Medline with the FDA for Lock-up.
| Device ID | K951736 |
| 510k Number | K951736 |
| Device Name: | LOCK-UP |
| Classification | Needle, Hypodermic, Single Lumen |
| Applicant | MEDLINE ONE MEDLINE PLACE Mundlelein, IL 60060 |
| Contact | Mary O'sullivan |
| Correspondent | Mary O'sullivan MEDLINE ONE MEDLINE PLACE Mundlelein, IL 60060 |
| Product Code | FMI |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-04-13 |
| Decision Date | 1995-07-05 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LOCK-UP 85024591 3935826 Live/Registered |
J.T. Eaton & Company, Inc. 2010-04-27 |
![]() LOCK-UP 77313818 3475391 Live/Registered |
Muscular Dystrophy Association, Inc. 2007-10-25 |
![]() LOCK-UP 74528196 not registered Dead/Abandoned |
K & S SPORTSWEAR INC. 1994-05-23 |
![]() LOCK-UP 73559646 1413811 Dead/Cancelled |
RAND INTERNATIONAL 1985-09-23 |