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

THROMBOLYTIC ASSESSMENT SYSTEM PROTHROMBIN TIME TEST CONTROLS

K Number: K961814 · Decision Aug 13, 1996
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
19
Applicant Total
13
Review Days
95

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Basic Information

Device Name
THROMBOLYTIC ASSESSMENT SYSTEM PROTHROMBIN TIME TEST CONTROLS
K Number
K961814
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cardiovascular Diagnostics, Inc.
Date Received
May 10, 1996
Decision Date
August 13, 1996
Product Code
GIZ
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
GIZ Plasma, Control, Normal

Similar 510(k) Clearances

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Other Clearances by Cardiovascular Diagnostics, Inc.

K Number Device Name
K013305 ENOXAPARIN TEST CARD
K994194 (TAS) LOW RANGE HEPARIN MANAGEMENT CARD RAPIDPOINT
K994159 HMP CONTROLS (TAS) RAPIDPOINT
K993519 RAPIDPOINT ACCENT, MODEL 2000, RAPIDPOINT COAG HEPARIN TITRATION TEST, RAPIDPOINT COAG PROTAMINE RESPONSE TEST
K990566 TAS ANALYZER, MODEL 1009
K981206 TAS RESULTS DATA ACQUISITION SYSTEM (TRAQS)
K981178 THROMBOLYTIC ASSESSMENT SYSTEM LOW RANGE HEPARIN MANAGEMENT TEST CONTROLS
K971748 TAS PT-NCTEST CONTROLS
K961189 TAS A PTT TEST CONTROLS
K960234 TAS HMT CONTROLS
Search all 13 clearances from Cardiovascular Diagnostics, Inc. →