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FDA 510(k) Application Details - K001718
Device Classification Name
Needle, Acupuncture, Single Use
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510(K) Number
K001718
Device Name
Needle, Acupuncture, Single Use
Applicant
UNITED PACIFIC CO., LTD.
219 SOUTH RAYMOND AVE.
ALHAMBRA, CA 91801 US
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Contact
DANIEL YE HUA
Other 510(k) Applications for this Contact
Regulation Number
880.5580
More FDA Info for this Regulation Number
Classification Product Code
MQX
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More FDA Info for this Product Code
Date Received
06/05/2000
Decision Date
06/21/2000
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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