International Technidyne Corp.
International Technidyne Corp. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 2013, with 1 FDA device recall on record.
Top product codes for International Technidyne Corp.
FDA recalls by International Technidyne Corp.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by International Technidyne Corp.
- K120977 — DIRECTCHECK CONTROL FOR HEMOCHRON JR. MICROCOAGULATION SYSTEMS ACT-LR CUVETTE DIRECTCHECK CONTROLS FOR HEMOCHRON JR. MIC
- K050016 — HEMOCHRON SIGNATURE ELITE
- K030818 — HEMOCHRON RESPONSE/SYSTEM
- K023561 — ITC HGB PRO PROFESSIONAL HEMOGLOBIN TESTING SYSTEM
- K020798 — HEMOCHRON JR. SIGNATURE +
- K010599 — PROTIME MICROCOAGULATION SYSTEM / PROTIME 3 CUVETTE
- K010193 — HEMOCHRON KAOLIN-ACTIVATED HEPARIN AND PROTAMINE DOSING ASSAYS
- K983475 — HEMOCHRON RESPONSE
- K990449 — HEMOCHRON ELECTRONIC SYSTEM VERIFICATION TUBE
- K972866 — HEMOCHRON JR. MIOCROCOAGULATION CITRATED PT
- K974799 — HEMOCHRON JR GENERATION II, HEMOCHRON JR SIGNATURE
- K972831 — HEMOCHRON CITRATE APTT
- K961835 — PROTIME MICROCOAGULATION SYSTEM
- K960749 — HEMOCHRON JR. MICROCOAGULATION LOW RANGE ACT
- K951072 — PROTIME MICROCOAGULATION SYSTEM
- K945078 — HEMOCHRON HNPT/FACTOR VI PT+
- K944691 — ITC WHOLE BLOOD CONTROL NORMAL/ABNORMAL LEVEL I OR II
- K940957 — HEMOCHRON VERIGY SYSTEM/FACTOR VI QUALIFY SYSTEM
- K941007 — CATALOG NO. J-ACT+ & QC-ACT+
- K941159 — DIRECTDRAW SUPERSERUM-G DIRECTDRAW SUPERSERUM-MINI-G
- K940432 — MICROCOAGULATION PROTHROMBIN TIME TEST
- K940401 — JR. MICROCOAGULATION SYSTEM
- K935081 — DIRECTDRAW SUPERSERUM-MINI
- K924637 — HEMOCHRON CITRA ONESTEP APTT/FAC VI SINGSHOT APTT
- K923302 — TENDERLETT FINGER
- K923761 — ITC MICROSAMPLE COAGULATION ANALYZER SYSTEM
- K924638 — HEMOCHRON DIRECT DRAW APTT/FAC VI VACU-APTT
- K923593 — HEMOCHRON/FACTOR VI FIBRINOGEN ASSAY AND CONT PLAS
- K921778 — DIRECTDRAW SUPERSERUM
- K915344 — HEMOCHRON ONESTEP APTT TEST
- K913861 — HEMOCHRON(R) KACT
- K911994 — HEMOCHRON(R) APTT, MODIFICATION
- K911995 — PROTHROMBIN TIME (PT) BY HEMOCHRON, MODIFICATION
- K911996 — SURGICUTT-BLEEDING TIME DEVICE, MODIFICATION
- K911997 — TENDERFOOT(R), MODIFICATION
- K910181 — HITT BY HEMOCHRON(R)
- K910646 — SUPERSERUM REAGENT (SSR)
- K910105 — PROTAMINE RESPONSE TEST CATALOGUE NUMBER PRT 200
- K904454 — HEMOCHRON(R) PROTHROMBIN TIME/MODIFICATION
- K900126 — TT AND HNTT BY HEMOCHRON
- K893378 — PROTHROMBIN TIME (PT) BY HEMOCHRON
- K883968 — TENDERFOOT
- K882480 — HEMOCHRON CONTROL PLASMA NORMAL/ABNORMAL LEV. I/II
- K882481 — HEMOCHRON CONTROL ACT TEST TUBE NORMAL/ABNOR. I/II
- K870831 — PDA699/PDA700 PROTAMINE DOSE ASSAY FOR HEP. NEUTRA
- K850542 — SURGICUTT - BLEEDING TIME DEVICE
- K832189 — HEMOCHRON THROMBOCHRONOMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.