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P900001 510(k) FDA Approval

P900001

None

FDA Premarket Approval P900001 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

DeviceP900001
Classification NameNone
Applicant
PMAP900001
SupplementS

Supplemental Filings

Supplement NumberDateSupplement Type
P900001Original Filing
S009 1993-05-11 Normal 180 Day Track
S008 1992-11-06 Normal 180 Day Track
S007 1992-09-23 Normal 180 Day Track
S006 1992-08-19 Normal 180 Day Track
S005 1992-03-04 Normal 180 Day Track
S004 1991-12-23 Normal 180 Day Track
S003 1991-07-16 Normal 180 Day Track
S002 1991-04-11 Normal 180 Day Track
S001 1991-02-08 30-Day Supplement

NIH GUDID Devices

Device IDPMASupp
00830002003019 P900001 001
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