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/ Electrophoresis Corp.
Electrophoresis Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K802395
SPECIAL PROCEDURE AQAROSE FILM
November 26, 1980
K790309
CPK ISOENZYME SUBSTRATE
April 4, 1979
K790310
HEMOGLOBIN CONTROLS
March 21, 1979
K790311
LDH ISOENZYME REAGENT
March 21, 1979