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FDA 510(k) Application Details - K955416
Device Classification Name
Electrocardiograph
More FDA Info for this Device
510(K) Number
K955416
Device Name
Electrocardiograph
Applicant
FUKUDA DENSHI USA, INC.
7102-A 180TH AVENUE NORTHEAST
REDMOND, WA 98052 US
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Contact
DAVID J GERAGHTY
Other 510(k) Applications for this Contact
Regulation Number
870.2340
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Classification Product Code
DPS
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More FDA Info for this Product Code
Date Received
11/27/1995
Decision Date
07/15/1996
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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