The following data is part of a premarket notification filed by Cheetah Medical Inc. with the FDA for Nicom.
Device ID | K042144 |
510k Number | K042144 |
Device Name: | NICOM |
Classification | Computer, Diagnostic, Pre-programmed, Single-function |
Applicant | CHEETAH MEDICAL INC. MIZPE AVIV, INDUSTRIAL PARK 13 M.p. Misgav, IL 20187 |
Contact | Benny Arazy |
Correspondent | Benny Arazy CHEETAH MEDICAL INC. MIZPE AVIV, INDUSTRIAL PARK 13 M.p. Misgav, IL 20187 |
Product Code | DXG |
CFR Regulation Number | 870.1435 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-08-09 |
Decision Date | 2004-11-12 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() NICOM 77073203 3316001 Dead/Cancelled |
CHEETAH MEDICAL, INC. 2006-12-29 |
![]() NICOM 76465187 2843712 Dead/Cancelled |
COBASYS LLC 2002-11-07 |
![]() NICOM 76324945 2699670 Dead/Cancelled |
WASHINGTON TRUST COMPANY 2001-10-15 |
![]() NICOM 76324710 2699667 Dead/Cancelled |
WASHINGTON TRUST COMPANY 2001-10-15 |
![]() NICOM 75871951 2398087 Live/Registered |
U.S. Chrome Corporation 1999-12-13 |
![]() NICOM 75552906 2307283 Dead/Cancelled |
Nicom Computers, Inc. 1998-09-14 |
![]() NICOM 74474883 1906312 Dead/Cancelled |
NICOM CORPORATION USA 1993-12-29 |