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 |