Myotronics-Noromed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Myotronics-Noromed, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Myotronics-Noromed, Inc. has 7 FDA 510(k) cleared medical devices. Based in Tukwila, US.
Historical record: 7 cleared submissions from 1999 to 2011. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Myotronics-Noromed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Myotronics-Noromed, Inc.
7 devices
Cleared
Sep 29, 2011
EMG SYSTEM
Neurology
105d
Cleared
Jul 20, 2004
MYO-TRODE SG DISPOSABLE ELECTRODE
Dental
154d
Cleared
Jul 24, 2003
MODEL J-5 MVO-MONITOR
Dental
27d
Cleared
Nov 13, 2001
MODEL MES-9000/EMG SYSTEM
Neurology
29d
Cleared
Nov 06, 2000
MODEL K7 EVALUATION DEVICE
Dental
17d
Cleared
Sep 10, 1999
MODIFICATION TO K6-I DIAGNOSTIC SYSTEM, MODEL K6-I
Dental
29d
Cleared
Aug 13, 1999
NORODYN 8000 SEMG SYSTEM, ND-8000
Neurology
22d