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FDA 510(k) Application Details - K963320
Device Classification Name
Wire, Guide, Catheter
More FDA Info for this Device
510(K) Number
K963320
Device Name
Wire, Guide, Catheter
Applicant
TFX MEDICAL GROUP
TALL PINES PARK
JAFFREY, NH 03452 US
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Contact
NEIL R ARMSTRONG
Other 510(k) Applications for this Contact
Regulation Number
870.1330
More FDA Info for this Regulation Number
Classification Product Code
DQX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/23/1996
Decision Date
12/03/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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