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FDA 510(k) Application Details - K980242
Device Classification Name
Assay, Heparin
More FDA Info for this Device
510(K) Number
K980242
Device Name
Assay, Heparin
Applicant
INSTRUMENTATION LABORATORY CO.
113 HARTWELL AVE.
LEXINGTON, MA 02173 US
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Contact
CAROL MARBLE
Other 510(k) Applications for this Contact
Regulation Number
864.7525
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Classification Product Code
KFF
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More FDA Info for this Product Code
Date Received
01/23/1998
Decision Date
03/19/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HE - Hematology
Review Advisory Committee
HE - Hematology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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