P010052S006

None

FDA Premarket Approval P010052 S006

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

DeviceP010052S006
Classification NameNone
Applicant
PMAP010052
SupplementS006

Supplemental Filings

Supplement NumberDateSupplement Type
P010052Original Filing
S016 2022-09-15 30-day Notice
S015
S014 2020-08-12 30-day Notice
S013 2019-11-25 30-day Notice
S012 2014-11-28 135 Review Track For 30-day Notice
S011 2011-12-19 135 Review Track For 30-day Notice
S010 2011-08-16 30-day Notice
S009 2011-08-08 30-day Notice
S008 2011-02-18 Real-time Process
S007 2009-11-02 Normal 180 Day Track No User Fee
S006
S005 2008-11-10 Normal 180 Day Track No User Fee
S004 2008-02-25 Normal 180 Day Track
S003 2005-08-17 Special (immediate Track)
S002
S001 2002-11-20 Real-time Process

NIH GUDID Devices

Device IDPMASupp
00630414982182 P010052 001
00630414970998 P010052 001

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