Grass-Telefactor Product Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Grass-Telefactor Product Group - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Grass-Telefactor Product Group has 12 FDA 510(k) cleared neurology devices. Based in W. Conshohocken, US.
Historical record: 12 cleared submissions from 1986 to 1999.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Grass-Telefactor Product Group
12 devices
Cleared
Aug 06, 1999
H20- TETHERED OPTION
Neurology
30d
Cleared
Jun 09, 1998
DEEGLITE
Neurology
203d
Cleared
Mar 09, 1998
H2O
Neurology
90d
Cleared
Jul 23, 1997
DEEG-LITE
Neurology
42d
Cleared
Apr 30, 1993
TELEFACTOR D/EEG-32
Neurology
163d
Cleared
Apr 14, 1989
BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING
Dental
137d
Cleared
May 08, 1987
A1-A2 AMBULATORY EEG CASSETTE RECORDER
Neurology
94d
Cleared
May 01, 1987
STD-228 SPECTRAL TREND DISPLAY
Neurology
17d
Cleared
Apr 08, 1987
SZAC-16 SEIZURE ANALYSIS COMPUTER
Neurology
64d
Cleared
Mar 25, 1987
DD-VCR-64
Neurology
55d
Cleared
Apr 17, 1986
SASSSY SEMI AUTOMATIC SLEEP SCORING SYSTEM
Neurology
85d
Cleared
Mar 27, 1986
MODAC-XXXX INTENSIVE MONITORING OF EEG
Neurology
72d