P200022S003

None

FDA Premarket Approval P200022 S003

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

DeviceP200022S003
Classification NameNone
Applicant
PMAP200022
SupplementS003

Supplemental Filings

Supplement NumberDateSupplement Type
P200022Original Filing
S004 2021-01-12 30-day Notice
S003
S002 2020-10-07 Normal 180 Day Track No User Fee
S001

NIH GUDID Devices

Device IDPMASupp
00843285101754 P200022 000
00843285100733 P200022 000
00843285100726 P200022 000
00843285100719 P200022 000
00843285100702 P200022 000
00843285100696 P200022 000
00843285100689 P200022 000
00843285100665 P200022 000
00843285100627 P200022 000
00843285100740 P200022 000
00843285100757 P200022 000
00843285100764 P200022 000
00843285101747 P200022 000
00843285101730 P200022 000
00843285100955 P200022 000
00843285100948 P200022 000
00843285100931 P200022 000
00843285100771 P200022 000
00843285100061 P200022 002
00843285100054 P200022 002
00843285100047 P200022 002
00843285100030 P200022 002
00843285100023 P200022 002
00843285100016 P200022 002
00843285100009 P200022 002
00843285100078 P200022 002
00843285100085 P200022 002
00843285100092 P200022 002
00843285100108 P200022 002
00843285100115 P200022 002
00843285100122 P200022 002
00843285100139 P200022 002
00843285101693 P200022 002
00843285101686 P200022 002
00843285101709 P200022 002

© 2021 FDA.report
This site is not affiliated with or endorsed by the FDA.