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

• Device: P020002S004
• Classification Name: None
• PMA: P020002
• Supplement: S004

Supplemental Filings

Supplement Number	Date	Supplement Type
P020002		Original 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 ID	PMA	Supp
15420045508163	P020002	000
15420045507265	P020002	000
15420045507258	P020002	000
15420045504103	P020002	000
15420045504097	P020002	000
15420045504080	P020002	000
15420045504042	P020002	000
15420045504035	P020002	000
15420045501041	P020002	000
15420045501034	P020002	000
15420045500990	P020002	000
15420045500983	P020002	000
15420045500976	P020002	000
15420045500945	P020002	000
15420045500938	P020002	000
15420045500921	P020002	000
15420045500914	P020002	000
15420045515062	P020002	000
15420045508156	P020002	000
15420045500938	P020002	007
15420045501034	P020002	007
15420045501041	P020002	007
15420045504035	P020002	007
15420045504042	P020002	007
15420045504080	P020002	007
15420045504097	P020002	007
15420045504103	P020002	007
15420045501027	P020002	007
15420045501010	P020002	007
15420045500921	P020002	007
15420045500945	P020002	007
15420045500907	P020002	007
15420045500891	P020002	007
15420045500976	P020002	007
15420045500983	P020002	007
15420045500990	P020002	007
15420045501003	P020002	007
15420045500914	P020002	007
15420045507258	P020002	010
15420045507265	P020002	010