The following data is part of a premarket notification filed by Instranetics, Inc. with the FDA for Line Caddy.
Device ID | K810294 |
510k Number | K810294 |
Device Name: | LINE CADDY |
Classification | Probe |
Applicant | INSTRANETICS, INC. 803 N. Front St. Suite 3 McHenry, IL 60050 |
Product Code | HXB |
CFR Regulation Number | 888.4540 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-02-04 |
Decision Date | 1981-02-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() LINE CADDY 90837718 not registered Live/Pending |
C-Pak, Inc. 2021-07-20 |
![]() LINE CADDY 75439894 2297500 Live/Registered |
C-PAK, INC. 1998-02-25 |