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FDA 510(k) Application Details - K002329
Device Classification Name
Pessary, Vaginal
More FDA Info for this Device
510(K) Number
K002329
Device Name
Pessary, Vaginal
Applicant
DESCHUTES MEDICAL PRODUCTS, INC.
1011 S.W. EMKAY DR., SUITE 104
BEND, OR 97702 US
Other 510(k) Applications for this Company
Contact
DENISE BESTWICK
Other 510(k) Applications for this Contact
Regulation Number
884.3575
More FDA Info for this Regulation Number
Classification Product Code
HHW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/01/2000
Decision Date
09/18/2000
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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