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FDA 510(k) Application Details - K011209
Device Classification Name
Needle, Conduction, Anesthetic (W/Wo Introducer)
More FDA Info for this Device
510(K) Number
K011209
Device Name
Needle, Conduction, Anesthetic (W/Wo Introducer)
Applicant
MANAN MEDICAL PRODUCTS, INC.
241 W. PALATINE RD.
WHEELING, IL 60090 US
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Contact
ROBBIE PALADUGU
Other 510(k) Applications for this Contact
Regulation Number
868.5150
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Classification Product Code
BSP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/19/2001
Decision Date
06/26/2001
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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