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P230020 510(k) FDA Approval

P230020

None

FDA Premarket Approval P230020 S

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

DeviceP230020
Classification NameNone
Applicant
PMAP230020
SupplementS

Supplemental Filings

Supplement NumberDateSupplement Type
P230020Original Filing

NIH GUDID Devices

Device IDPMASupp
00810118490095 P230020 000
00810118490088 P230020 000
00810118490071 P230020 000
00810118490064 P230020 000
00810118490057 P230020 000
00810118490026 P230020 000
00810118490019 P230020 000
00810118490002 P230020 000
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