ClearanceBrief
Company ยท US

Grass Instrument Co.

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 2002. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OLVStandard Polysomnograph With Electroencephalograph2
GWEStimulator, Photic, Evoked Response1
GWJStimulator, Auditory, Evoked Response1
GWKConditioner, Signal, Physiological1
JXEDevice, Nerve Conduction Velocity Measurement1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 29, 2002K021807GRASS-TELEFACTOR AS40 AMPLIFIER SYSTEM
Grass Instrument Co.
OLV
Mar 6, 2000K994142GRASS TS3201/6401 EEG AMPLIFIER SYSTEM
Grass Instrument Co.
OLV
Jan 18, 1985K844216GRASS MODEL NL FACIAL NERVE LOCATOR & MONITOR
Grass Instrument Co.
JXE
Aug 20, 1981K812061MODEL S10VS VISUAL STIMULATOR
Grass Instrument Co.
GWE
Mar 17, 1981K810539MODEL S10CTCM AUDITORY STIMULATOR
Grass Instrument Co.
GWJ
Nov 22, 1977K771742EVOKED RESPONSE SYS., MODEL 10
Grass Instrument Co.
GWK

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes