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FDA 510(k) Application Details - K160502
Device Classification Name
System, Multipurpose For In Vitro Coagulation Studies
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510(K) Number
K160502
Device Name
System, Multipurpose For In Vitro Coagulation Studies
Applicant
Haemonetics Corporation
400 Wood Road
Braintree, MA 02184 US
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Contact
Paige Sweeney
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Regulation Number
864.5425
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Classification Product Code
JPA
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More FDA Info for this Product Code
Date Received
02/23/2016
Decision Date
04/19/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HE - Hematology
Review Advisory Committee
HE - Hematology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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