Diagnostic Technology, Inc.
Diagnostic Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1991.
Top product codes for Diagnostic Technology, Inc.
Recent clearances by Diagnostic Technology, Inc.
- K896378 — LYME-CHECK(TM) TEST KIT
- K903612 — EBV/EA-CHECK TM TEST KIT
- K890639 — RESUBMITTED EBV/IGM-CHECK TEST KIT
- K890819 — HSV-CHECK(TM) TEST KIT
- K891542 — EBNA-CHECK(TM) TEST KIT
- K871373 — EBV-CHECK(TM) TEST KIT (IGG)
- K864128 — CHLAMYDIA-CHECK(TM) DIRECT & CULTURE CONFIR. KIT
- K863408 — EBV/VCA-CHECK(TM) ANTIGEN SLIDES
- K860586 — PHA-2 CONVERSION PROGRAM FOR PLATELET ANALYSIS
- K860166 — PICOSCALE BLOOD CELL COUNTER, MODEL PS-5
- K853036 — PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1
- K841809 — COUNT-A-PART PLUS
- K842140 — PICOSCAL BLOOD CELL COUNTER PS-4
- K834345 — IM-CHECK
- K834372 — PHA-1 PROGRAMMABLE HEMATOLOGY ANALYZ
- K834346 — BHCG-CHECK
- K831466 — HCG-CHECK
- K831468 — B HCG-CHECK
- K831464 — ASO-CHECK
- K831463 — ANA-CHECK
- K831465 — CRP-CHECK
- K831467 — RA-CHECK
- K827289 — DIGITAL RADIOGRAPHY SYSTEM
- K820037 — SICKLE-CHECK
- K811063 — LASER-CAL
- K791750 — COUNTER-CHECK PLUS
- K791772 — COUNTER-CHECK PLUS NORMAL, HIGH ABN.
- K790025 — COUNTER CHECK, H001, H002, H003
Data sourced from openFDA. This site is unofficial and independent of the FDA.