FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HEMOCHRON(R) PROTHROMBIN TIME/MODIFICATION

K Number: K904454 · Decision Dec 17, 1990
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
124
Applicant Total
47
Review Days
91

Basic Information

Device Name
HEMOCHRON(R) PROTHROMBIN TIME/MODIFICATION
K Number
K904454
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7750
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
INTERNATIONAL TECHNIDYNE CORP.
Date Received
September 17, 1990
Decision Date
December 17, 1990
Product Code
GJS
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GJS Test, Time, Prothrombin

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Other Clearances by INTERNATIONAL TECHNIDYNE CORP.

K Number Device Name
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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
Search all 47 clearances from INTERNATIONAL TECHNIDYNE CORP. →