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FDA 510(k) Application Details - K992126
Device Classification Name
Apparatus, Suction, Operating-Room, Wall Vacuum Powered
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510(K) Number
K992126
Device Name
Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Applicant
CIRCON CORP.
6500 HOLLISTER AVE.
SANTA BARBARA, CA 93117-3019 US
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Contact
RONALD J EHMSEN
Other 510(k) Applications for this Contact
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
06/23/1999
Decision Date
08/03/1999
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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