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FDA 510(k) Application Details - K994059
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K994059
Device Name
Anesthesia Conduction Kit
Applicant
HDC CORP.
2109 O'TOOLE AVE.
SAN JOSE, CA 95131 US
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Contact
JAMES ABILLA
Other 510(k) Applications for this Contact
Regulation Number
868.5140
More FDA Info for this Regulation Number
Classification Product Code
CAZ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/29/1999
Decision Date
10/13/2000
Decision
SESE - SUBST EQUIV
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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