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FDA 510(k) Application Details - K974000
Device Classification Name
Kinetic Method, Gamma-Glutamyl Transpeptidase
More FDA Info for this Device
510(K) Number
K974000
Device Name
Kinetic Method, Gamma-Glutamyl Transpeptidase
Applicant
DIAGNOSTIC CHEMICALS LTD.
WEST ROYALTY INDUSTRIAL PARK,
CHARLOTTETOWN, P.E.I. C1E 2A6 CA
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Contact
KAREN CALLBECK
Other 510(k) Applications for this Contact
Regulation Number
862.1360
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Classification Product Code
JQB
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More FDA Info for this Product Code
Date Received
10/21/1997
Decision Date
11/04/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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