P200022S001

None

FDA Premarket Approval P200022 S001

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

DeviceP200022S001
Classification NameNone
Applicant
PMAP200022
SupplementS001

Supplemental Filings

Supplement NumberDateSupplement Type
P200022Original Filing
S008 2022-01-14 30-day Notice
S007 2021-06-25 30-day Notice
S006 2021-04-29 Normal 180 Day Track No User Fee
S005 2021-04-28 Normal 180 Day Track No User Fee
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
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00843285100078 P200022 002

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