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FDA 510(k) Application Details - K993619
Device Classification Name
Needle, Conduction, Anesthetic (W/Wo Introducer)
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510(K) Number
K993619
Device Name
Needle, Conduction, Anesthetic (W/Wo Introducer)
Applicant
SIMS PORTEX, INC.
10 BOWMAN DR.
KEENE, NH 03431 US
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Contact
TIMOTHY J TALCOTT
Other 510(k) Applications for this Contact
Regulation Number
868.5150
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Classification Product Code
BSP
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More FDA Info for this Product Code
Date Received
10/26/1999
Decision Date
04/28/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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