This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P040025S001 |
Classification Name | None |
Applicant | |
PMA | P040025 |
Supplement | S001 |
Supplement Number | Date | Supplement Type |
---|---|---|
P040025 | Original Filing | |
S014 | 2013-06-26 | Normal 180 Day Track No User Fee |
S013 | 2013-05-28 | Normal 180 Day Track |
S012 | 2012-01-26 | Real-time Process |
S011 | 2010-09-29 | Real-time Process |
S010 | 2010-05-03 | Real-time Process |
S009 | 2009-07-21 | Real-time Process |
S008 | 2008-10-27 | Real-time Process |
S007 | 2008-07-16 | Normal 180 Day Track |
S006 | 2007-10-24 | Real-time Process |
S005 | 2007-08-24 | 30-day Notice |
S004 | ||
S003 | ||
S002 | ||
S001 |
Device ID | PMA | Supp |
---|---|---|
00382830016308 | P040025 | 000 |
00382830009584 | P040025 | 000 |
00382830009577 | P040025 | 000 |
00382830009560 | P040025 | 000 |
00382830004169 | P040025 | 000 |