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FDA 510(k) Application Details - K042454
Device Classification Name
Apparatus, Suction, Operating-Room, Wall Vacuum Powered
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510(K) Number
K042454
Device Name
Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Applicant
Stryker Endoscopy
5900 OPTICAL CT.
SAN JOSE, CA 95138 US
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Contact
CHRISTOPHER L COOK
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Regulation Number
880.6740
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Classification Product Code
GCX
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More FDA Info for this Product Code
Date Received
09/10/2004
Decision Date
12/09/2004
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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