Grass Instrument Co. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Grass Instrument Co. Neurology ✕
6 devices
Cleared
Aug 29, 2002
GRASS-TELEFACTOR AS40 AMPLIFIER SYSTEM
Neurology
87d
Cleared
Mar 06, 2000
GRASS TS3201/6401 EEG AMPLIFIER SYSTEM
Neurology
89d
Cleared
Jan 18, 1985
GRASS MODEL NL FACIAL NERVE LOCATOR & MONITOR
Neurology
79d
Cleared
Aug 20, 1981
MODEL S10VS VISUAL STIMULATOR
Neurology
30d
Cleared
Mar 17, 1981
MODEL S10CTCM AUDITORY STIMULATOR
Neurology
18d
Cleared
Nov 22, 1977
EVOKED RESPONSE SYS., MODEL 10
Neurology
68d