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FDA 510(k) Application Details - K972282
Device Classification Name
Detector And Alarm, Arrhythmia
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510(K) Number
K972282
Device Name
Detector And Alarm, Arrhythmia
Applicant
SPACELABS MEDICAL, INC.
P.O. BOX 97013
REDMOND, WA 98073-9713 US
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Contact
RUSS GARRSION
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Regulation Number
870.1025
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Classification Product Code
DSI
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More FDA Info for this Product Code
Date Received
06/18/1997
Decision Date
09/25/1997
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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