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FDA 510(k) Application Details - K002910
Device Classification Name
Needle, Acupuncture, Single Use
More FDA Info for this Device
510(K) Number
K002910
Device Name
Needle, Acupuncture, Single Use
Applicant
ANC IMPORT & EXPORT CO. LTD.
4309 MURWICK DR.
ARLINGTON, TX 76016 US
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Contact
WILLIAM ZHANG
Other 510(k) Applications for this Contact
Regulation Number
880.5580
More FDA Info for this Regulation Number
Classification Product Code
MQX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/18/2000
Decision Date
02/07/2001
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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