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

RAPIDTEG TEG-ACT TEST

K Number: K062604 · Decision Jan 31, 2007
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
23
Applicant Total
7
Review Days
152

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Basic Information

Device Name
RAPIDTEG TEG-ACT TEST
K Number
K062604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7140
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Haemoscope Corp.
Date Received
September 1, 2006
Decision Date
January 31, 2007
Product Code
JBP
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
JBP Activated Whole Blood Clotting Time

Similar 510(k) Clearances

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

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Other Clearances by Haemoscope Corp.

K Number Device Name
K041502 THROMBELASTOGRAPH (TEG) PLATELET MAPPING ASSAY
K002177 THROMBELASTOGRAPH COAGULATION ANALYZER TEG-5000 SERIES
K993678 THROMBELASTOGRAPH COAGULATION ANALYZER TEG - 5000 SERIES
K954437 THROMBELASTOGRAPH COAGULATION ANALYZER 3000S
K904204 THROMBELASTOGRAPH
K895844 THROMBELASTOGRAPH(R)