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FDA 510(k) Application Details - K001129
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K001129
Device Name
Anesthesia Conduction Kit
Applicant
LIFE-TECH INTL., INC.
4235 GREENBRIAR DR.
STAFFORD, TX 77477-3995 US
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Contact
JEFF KASOFF
Other 510(k) Applications for this Contact
Regulation Number
868.5140
More FDA Info for this Regulation Number
Classification Product Code
CAZ
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More FDA Info for this Product Code
Date Received
04/07/2000
Decision Date
07/06/2000
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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