Medical Device Manufacturer · US , Mchenry , IL

Diagnostic Technology, Inc. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1979

Total

Cleared

Denied

Diagnostic Technology, Inc. has 28 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 28 cleared submissions from 1979 to 1991.

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

FDA 510(k) Regulatory Record - Diagnostic Technology, Inc.

28 devices

1-12 of 28

Cleared Nov 05, 1991

LYME-CHECK(TM) TEST KIT

K896378 · LSR

Microbiology · 729d

Cleared Oct 16, 1990

EBV/EA-CHECK TM TEST KIT

K903612 · LSE

Microbiology · 68d

Cleared Jun 20, 1989

RESUBMITTED EBV/IGM-CHECK TEST KIT

K890639 · LJN

Microbiology · 132d

Cleared Jun 20, 1989

HSV-CHECK(TM) TEST KIT

K890819 · HIS

Microbiology · 123d

Cleared Jun 20, 1989

EBNA-CHECK(TM) TEST KIT

K891542 · LLM

Microbiology · 95d

Cleared Jun 25, 1987

EBV-CHECK(TM) TEST KIT (IGG)

K871373 · GNP

Microbiology · 79d

Cleared Apr 29, 1987

CHLAMYDIA-CHECK(TM) DIRECT & CULTURE CONFIR. KIT

K864128 · LJP

Microbiology · 190d

Cleared Nov 28, 1986

EBV/VCA-CHECK(TM) ANTIGEN SLIDES

K863408 · GNP

Microbiology · 86d

Cleared May 07, 1986

PHA-2 CONVERSION PROGRAM FOR PLATELET ANALYSIS

K860586 · GKL

Hematology · 77d

Cleared Apr 04, 1986

PICOSCALE BLOOD CELL COUNTER, MODEL PS-5

K860166 · GKL

Hematology · 77d

Cleared Nov 05, 1985

PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1

Diagnostic Technology, Inc. - FDA 510(k) Cleared Devices

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