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FDA 510(k) Application Details - K961694
Device Classification Name
Station, Pipetting And Diluting, For Clinical Use
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510(K) Number
K961694
Device Name
Station, Pipetting And Diluting, For Clinical Use
Applicant
MATRIX TECHNOLOGIES CORP.
44 STEDMAN ST.
LOWELL, MA 01851 US
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Contact
MAR HAMEL
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Regulation Number
862.2750
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Classification Product Code
JQW
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More FDA Info for this Product Code
Date Received
05/01/1996
Decision Date
06/21/1996
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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