Electrophoresis Corp. of America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Electrophoresis Corp. of America - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Electrophoresis Corp. of America has 27 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 27 cleared submissions from 1978 to 1980.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Electrophoresis Corp. of America
27 devices
Cleared
Nov 26, 1980
GENERAL PROCEDURE AGAROSE FILM
Chemistry
55d
Cleared
Jan 29, 1980
AGAROSE BARBITAL BUFFER
Chemistry
50d
Cleared
Jan 29, 1980
ALKALINE PHOSPHATASE MARKER
Chemistry
50d
Cleared
Jan 29, 1980
ALKALINE PHOSPHATASE REAGENT
Chemistry
50d
Cleared
Jan 29, 1980
AGAROSE BARBITAL-EDTA BUFFER
Chemistry
50d
Cleared
Jan 21, 1980
MOPSO BUFFER
Pathology
39d
Cleared
Jan 16, 1980
PONCEAU S STAIN SET
Hematology
37d
Cleared
Dec 18, 1979
FAT RED 7B STAIN SET
Pathology
8d
Cleared
Dec 18, 1979
AMIDO BLACK 10B STAIN
Pathology
8d
Cleared
Sep 17, 1979
NORMAL CONTROL
Chemistry
27d
Cleared
Sep 17, 1979
CPK ISOENZYME REAGENT
Chemistry
27d
Cleared
Sep 17, 1979
ENZYME STABILIZING REAGENT (ESR)
Chemistry
27d