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

HMP CONTROLS (TAS) RAPIDPOINT

K Number: K994159 · Decision Feb 15, 2000
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
98
Applicant Total
13
Review Days
68

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Basic Information

Device Name
HMP CONTROLS (TAS) RAPIDPOINT
K Number
K994159
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
December 9, 1999
Decision Date
February 15, 2000
Product Code
GGN
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
GGN Plasma, Coagulation Control

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GGN), ordered by most recent decision date.

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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
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
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. →