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FDA 510(k) Application Details - K102480
Device Classification Name
Microtools, Assisted Reproduction (Pipettes)
More FDA Info for this Device
510(K) Number
K102480
Device Name
Microtools, Assisted Reproduction (Pipettes)
Applicant
JIEYING LABORATORY INC.
9722 AVE. SAUSALITO
IRVINE, CA 92606 US
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Contact
GRACE HOLLAND
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Regulation Number
884.6130
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Classification Product Code
MQH
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More FDA Info for this Product Code
Date Received
08/30/2010
Decision Date
04/19/2011
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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