Medical Device Manufacturer · US , Mchenry , IL

Coulter Electronics, Inc. - FDA 510(k) Cleared Devices

101 submissions · 101 cleared · Since 1976

101

Total

101

Cleared

Denied

Coulter Electronics, Inc. has 101 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 101 cleared submissions from 1976 to 1994. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Coulter Electronics, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Coulter Electronics, Inc.

101 devices

1-12 of 101

COULTER RETIC-C CELL CONTROL

COULTER MAXM W/ AUTOLOADER

PX COULTER(R) CELL CONTROL

COULTER DART AST (GOT) REAGENT

K905771 · CIT

Chemistry · 61d

Cleared Jan 25, 1991

COULTER DART ALT (GPT) REAGENT

K905767 · CKA

Chemistry · 29d

Cleared Dec 26, 1990

COULTER DIRECT BILLRUBIN REAGENT

K905622 · CIG

Chemistry · 12d

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Coulter Electronics, Inc. - FDA 510(k) Cleared Devices

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