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FDA 510(k) Application Details - K162563
Device Classification Name
Catheter, Percutaneous
More FDA Info for this Device
510(K) Number
K162563
Device Name
Catheter, Percutaneous
Applicant
CODMAN & SHURTLEFF, INC.
325 PARAMOUNT DRIVE
RAYNHAM, MA 02767 US
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Contact
YOON HEE BEATTY
Other 510(k) Applications for this Contact
Regulation Number
870.1250
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Classification Product Code
DQY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/14/2016
Decision Date
01/05/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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