Myo-Tronics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Myo-Tronics, Inc. - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
Myo-Tronics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 5 cleared submissions from 1991 to 1997. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Myo-Tronics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Myo-Tronics, Inc.
6 devices
Cleared
Apr 02, 1997
ESG-1 ELECTROSONOGRAM (ESG-1)
Dental
79d
Cleared
Dec 09, 1994
K6-1 DIAGNOSTIC SYSTEM VERSION 3.1
Dental
107d
Cleared
Sep 02, 1994
PHYSIOTECH 4000 OR NORODYN 8000
Neurology
841d
Cleared
Jun 09, 1994
K6-I DIAGNOSTIC SYSTEM
Dental
744d
Cleared
Jan 07, 1993
MS-100 MYO-SCANNER OR MS-100 EMG SCANNER
Dental
259d
Cleared
Apr 26, 1991
ELECTROSONOGRAM ESG-1
Dental
142d