Chester Labs, Inc. is one of 22788 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chester Labs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: E-Z LUBRICATING JELLY, STATSIGN ELECTRODE CONDUCTIVITY GEL, GRAHAM-FIELD ELECTRODE CONDUCTIVITY GEL, MODELS 004008, 48-4000 2GF, 48-4000GF, MODIFICATION TO STATSIGN SALINE ELECTROLYTE GEL, GRAHAM-FIELD SALINE ELECTROLYTE GEL
11
Total
11
Cleared
0
Denied
Chester Labs, Inc. has 11 FDA 510(k) cleared medical devices. Based in Erlanger, US.
Historical record: 11 cleared submissions from 1985 to 2004. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Chester Labs, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Chester Labs, Inc.
11 devices
Cleared
May 07, 2004
E-Z LUBRICATING JELLY
General Hospital
14d
Cleared
Jun 29, 2000
STATSIGN ELECTRODE CONDUCTIVITY GEL, GRAHAM-FIELD ELECTRODE CONDUCTIVITY GEL,...
Neurology
24d
Cleared
Jun 14, 2000
MODIFICATION TO STATSIGN SALINE ELECTROLYTE GEL, GRAHAM-FIELD SALINE...
General & Plastic Surgery
22d
Cleared
May 07, 1996
GRAHAM-FIELD ELECTRODE CONDUCTIVITY GEL
Neurology
596d
Cleared
May 07, 1996
GRAHAM-FIELD CONDUCTIVE ECG SPRAY
Neurology
596d
Cleared
Nov 20, 1995
GRAHAM-FIELD SALINE ELECTROLYTE GEL
Neurology
427d
Cleared
Jun 21, 1995
GRAHAM-FIELD ULTRASOUND SCANNING GEL
Radiology
275d
Cleared
Jun 07, 1995
GRAHAM-FIELD ULTRASOUND LOTION
Radiology
261d
Cleared
Mar 23, 1994
BIOSHIELD BLUE POWDER FREE GLOVE
General Hospital
61d
Cleared
Mar 23, 1994
BIOSHIELD BLUE LATEX GLOVES
General Hospital
61d
Cleared
Mar 14, 1985
LIQUA-SONIC GEL
Neurology
311d