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FDA 510(k) Application Details - K955817
Device Classification Name
Catheter, Electrode Recording, Or Probe, Electrode Recording
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510(K) Number
K955817
Device Name
Catheter, Electrode Recording, Or Probe, Electrode Recording
Applicant
CORDIS WEBSTER, INC.
4750 LITTLEJOHN ST.
BALDWIN PARK, CA 91706 US
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Contact
MARY ADAMS
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Regulation Number
870.1220
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Classification Product Code
DRF
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More FDA Info for this Product Code
Date Received
12/26/1995
Decision Date
03/25/1996
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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