P050031S008

None

FDA Premarket Approval P050031 S008

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

DeviceP050031S008
Classification NameNone
Applicant
PMAP050031
SupplementS008

Supplemental Filings

Supplement NumberDateSupplement Type
P050031Original Filing
S009 2022-04-15 30-day Notice
S008
S007 2020-08-05 30-day Notice
S006 2020-08-04 30-day Notice
S005 2019-03-13 Normal 180 Day Track No User Fee
S004
S003 2019-02-04 Real-time Process
S002
S001 2010-10-25 Normal 180 Day Track No User Fee

NIH GUDID Devices

Device IDPMASupp
B22222 P050031 000
B22221 P050031 000

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