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FDA 510(k) Application Details - K024290
Device Classification Name
Media, Reproductive
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510(K) Number
K024290
Device Name
Media, Reproductive
Applicant
CERES FERTILITY, INC.
3722 AVE. SAUSALITO
IRVINE, CA 92606 US
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Contact
GRACE HOLLAND
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Regulation Number
884.6180
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Classification Product Code
MQL
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More FDA Info for this Product Code
Date Received
12/23/2002
Decision Date
03/03/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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