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

ACL TOP

K Number: K063679 · Decision Jan 12, 2007
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
48
Applicant Total
321
Review Days
32

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Basic Information

Device Name
ACL TOP
K Number
K063679
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
864.5400
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Instrumentation Laboratory CO
Date Received
December 11, 2006
Decision Date
January 12, 2007
Product Code
GKP
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
GKP Instrument, Coagulation, Automated

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