International Technidyne Corp. is one of 5191 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
International Technidyne Corp. - FDA 510(k) Cleared Devices
47
Total
47
Cleared
0
Denied
International Technidyne Corp. has 47 FDA 510(k) cleared hematology devices. Based in Walker, US.
Historical record: 47 cleared submissions from 1983 to 2013.
Browse the complete list of FDA 510(k) cleared hematology devices from this manufacturer. Filter by specialty or product code using the sidebar.
International Technidyne Corp. — FDA 510(k) Products and Clearance History
47 devices
Cleared
Jul 03, 2013
DIRECTCHECK CONTROL FOR HEMOCHRON JR. MICROCOAGULATION SYSTEMS ACT-LR CUVETTE...
Hematology
457d
Cleared
Feb 10, 2005
HEMOCHRON SIGNATURE ELITE
Hematology
37d
Cleared
Apr 02, 2003
HEMOCHRON RESPONSE/SYSTEM
Hematology
19d
Cleared
Jan 31, 2003
ITC HGB PRO PROFESSIONAL HEMOGLOBIN TESTING SYSTEM
Hematology
100d
Cleared
Mar 28, 2002
HEMOCHRON JR. SIGNATURE +
Hematology
16d
Cleared
Jul 02, 2001
PROTIME MICROCOAGULATION SYSTEM / PROTIME 3 CUVETTE
Hematology
124d
Cleared
Jun 06, 2001
HEMOCHRON KAOLIN-ACTIVATED HEPARIN AND PROTAMINE DOSING ASSAYS
Hematology
135d
Cleared
May 03, 1999
HEMOCHRON RESPONSE
Hematology
213d
Cleared
Apr 13, 1999
HEMOCHRON ELECTRONIC SYSTEM VERIFICATION TUBE
Hematology
60d
Cleared
Sep 30, 1998
HEMOCHRON JR. MIOCROCOAGULATION CITRATED PT
Hematology
422d
Cleared
Jul 07, 1998
HEMOCHRON JR GENERATION II, HEMOCHRON JR SIGNATURE
Hematology
197d
Cleared
Nov 20, 1997
HEMOCHRON CITRATE APTT
Hematology
113d
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