Eaton Medical Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eaton Medical Group - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Eaton Medical Group has 15 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 15 cleared submissions from 1983 to 1986.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eaton Medical Group
15 devices
Cleared
Jan 22, 1986
MODEL TRC-40 TELEMETRY RECIEVER MODULE
Cardiovascular
279d
Cleared
Jan 14, 1986
MODEL TT-185 TELEMETRY TRANSMITTER
Cardiovascular
271d
Cleared
Nov 19, 1985
SCX-10 SINGLE CHANNEL RECORDER ACCESS. FOR G-2000
Cardiovascular
215d
Cleared
Nov 08, 1985
KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR
Cardiovascular
204d
Cleared
Nov 08, 1985
PCX-100 PATIENT INPUT LEADWIRE
Cardiovascular
204d
Cleared
Jul 15, 1985
TMX-C1/C2 TRADMILL CONTROLLER ACCESS.
Physical Medicine
88d
Cleared
Jul 09, 1985
TMX-70 TREADMILL
Physical Medicine
82d
Cleared
Jul 09, 1985
TMX-80 TREADMILL
Physical Medicine
82d
Cleared
Jun 27, 1985
RMG-9 9 REMOTE MONITOR ACCESS. FOR G-2000 ELECTRO
Cardiovascular
70d
Cleared
Jun 26, 1985
SCX-35 THREE CHANNEL ACCESS. FOR MODULE G-2000 ELE
Cardiovascular
69d
Cleared
Jun 26, 1985
CC-100 CLOCK/CALANDER MODULE ACCESS. FOR G-2000 EL
Cardiovascular
69d
Cleared
May 16, 1985
RESTING ECG SOFTWARE FRO G-2000 ELECTROCARDIOGRAPH
Cardiovascular
108d
Cleared
May 16, 1985
TELEMETRY SOFTWARE FOR G-2000 ELECTROCARDIOGRAPH
Cardiovascular
108d
Cleared
Apr 09, 1985
RECORDING ACCESSORY FOR G-2000 EKG MACH. GMP-40 RE
Cardiovascular
69d
Cleared
Dec 01, 1983
G-2000
Cardiovascular
146d