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FDA 510(k) Application Details - K955339
Device Classification Name
Catheter, Irrigation
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510(K) Number
K955339
Device Name
Catheter, Irrigation
Applicant
NORTHGATE TECHNOLOGIES, INC.
600 CHURCH RD.
ELGIN, IL 60123 US
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Contact
CASEY KUREK
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Regulation Number
878.4200
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Classification Product Code
GBX
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More FDA Info for this Product Code
Date Received
11/20/1995
Decision Date
03/13/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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