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

RAPIDPOINT ACCENT, MODEL 2000, RAPIDPOINT COAG HEPARIN TITRATION TEST, RAPIDPOINT COAG PROTAMINE RESPONSE TEST

K Number: K993519 · Decision Jan 14, 2000
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
14
Applicant Total
13
Review Days
88

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Basic Information

Device Name
RAPIDPOINT ACCENT, MODEL 2000, RAPIDPOINT COAG HEPARIN TITRATION TEST, RAPIDPOINT COAG PROTAMINE RESPONSE TEST
K Number
K993519
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5680
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cardiovascular Diagnostics, Inc.
Date Received
October 18, 1999
Decision Date
January 14, 2000
Product Code
JOX
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
JOX Analyzer, Heparin, Automated

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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
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
K961814 THROMBOLYTIC ASSESSMENT SYSTEM PROTHROMBIN TIME TEST CONTROLS
K961189 TAS A PTT TEST CONTROLS
K960234 TAS HMT CONTROLS
Search all 13 clearances from Cardiovascular Diagnostics, Inc. →