P020002S004

None

FDA Premarket Approval P020002 S004

This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.

Pre-market Approval Supplement Details

DeviceP020002S004
Classification NameNone
Applicant
PMAP020002
SupplementS004

Supplemental Filings

Supplement NumberDateSupplement Type
P020002Original Filing
S010 2014-11-14 Normal 180 Day Track
S009 2014-10-16 Real-time Process
S008 2014-06-20 Real-time Process
S007 2014-01-30 Real-time Process
S006 2011-11-29 Real-time Process
S005 2010-08-19 Special (immediate Track)
S004
S003 2007-07-11 Normal 180 Day Track No User Fee
S002 2006-03-30 Real-time Process
S001 2005-05-03 Normal 180 Day Track No User Fee

NIH GUDID Devices

Device IDPMASupp
15420045508163 P020002 000
15420045500990 P020002 000
15420045501034 P020002 000
15420045501041 P020002 000
15420045504097 P020002 000
15420045504035 P020002 000
15420045504042 P020002 000
15420045504080 P020002 000
15420045504103 P020002 000
15420045507258 P020002 000
15420045500983 P020002 000
15420045500976 P020002 000
15420045500945 P020002 000
15420045508156 P020002 000
15420045507265 P020002 000
15420045500921 P020002 000
15420045515062 P020002 000
15420045500914 P020002 000
15420045500938 P020002 000
15420045515062 P020002 006
15420045504097 P020002 007
15420045500976 P020002 007
15420045508156 P020002 007
15420045508163 P020002 007
15420045500891 P020002 007
15420045504103 P020002 007
15420045504080 P020002 007
15420045504042 P020002 007
15420045504035 P020002 007
15420045501041 P020002 007
15420045501034 P020002 007
15420045501027 P020002 007
15420045501010 P020002 007
15420045501003 P020002 007
15420045500907 P020002 007
15420045500914 P020002 007
15420045500921 P020002 007
15420045500938 P020002 007
15420045500945 P020002 007
15420045500983 P020002 007
15420045500990 P020002 007
15420045507258 P020002 010
15420045507265 P020002 010

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