The following data is part of a premarket notification filed by B. Braun Instruments with the FDA for Connectors.
| Device ID | K760382 |
| 510k Number | K760382 |
| Device Name: | CONNECTORS |
| Classification | Connector, Catheter |
| Applicant | B. BRAUN INSTRUMENTS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GCD |
| CFR Regulation Number | 878.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-05 |
| Decision Date | 1976-11-02 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CONNECTORS 86755083 not registered Dead/Abandoned |
JAKKS Pacific, Inc. 2015-09-12 |
![]() CONNECTORS 76474834 not registered Dead/Abandoned |
Bolt, Inc. 2002-12-10 |
![]() CONNECTORS 75776457 2366357 Live/Registered |
Junot Systems, Inc. 1999-08-16 |
![]() CONNECTORS 74507570 1926392 Live/Registered |
SERFAS, INC. 1994-03-31 |
![]() CONNECTORS 73787727 1564704 Dead/Cancelled |
K MART CORPORATION 1989-03-20 |