Mennen Greatbatch Electonics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mennen Greatbatch Electonics - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Mennen Greatbatch Electonics has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1977 to 1977. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mennen Greatbatch Electonics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mennen Greatbatch Electonics
6 devices
Cleared
Nov 22, 1977
ECG TELEMETRY SYSTEM
Cardiovascular
32d
Cleared
Jun 03, 1977
PORTASCOPE II
Cardiovascular
28d
Cleared
Feb 24, 1977
MONITOR, PORTABLE, PART #431-010
Cardiovascular
10d
Cleared
Feb 14, 1977
ABDOMINAL FETAL ECG MODULE
Obstetrics & Gynecology
7d
Cleared
Feb 14, 1977
ISOLATED EEG AMPLIFIER MODULE
Neurology
7d
Cleared
Feb 14, 1977
D.C. AMPLIFIER MODULE
Cardiovascular
7d