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.

Diagnostic Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

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

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