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FDA 510(k) Application Details - K962880
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K962880
Device Name
Anesthesia Conduction Kit
Applicant
SHERWOOD MEDICAL CO.
1915 OLIVE ST.
ST. LOUIS, MO 63103-1642 US
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Contact
DENNIS POZZO
Other 510(k) Applications for this Contact
Regulation Number
868.5140
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Classification Product Code
CAZ
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More FDA Info for this Product Code
Date Received
07/24/1996
Decision Date
12/09/1996
Decision
SESK - SUBST EQUIV - KIT
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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