This page includes the latest FDA filings for Popper Sons Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
POPPER & SONS, INC. | HYPODERMIC NEEDLES, SINGLE LUMEN | 1991-05-20 |
POPPER & SONS, INC. | J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI | 1984-10-26 |
POPPER & SONS, INC. | ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE | 1984-10-25 |
POPPER & SONS, INC. | WESCOTT TYPE BIOPSY NEEDLE | 1984-08-09 |
POPPER & SONS, INC. | GARDNER TYPE BONE MARROW NEEDLE | 1984-06-05 |
POPPER & SONS, INC. | ANTRUM NEEDLE-WOLF TYPE | 1984-06-05 |
POPPER & SONS, INC. | BIERMAN BIOPSY NEEDLE | 1984-05-02 |
POPPER & SONS, INC. | WESTERMAN-JENSEN BIOPSY NEEDLE | 1984-03-12 |
NCAGE Code | 95388 | POPPER & SONS INC. |
CAGE Code | 95388 | POPPER & SONS, INC. |
DUNS | 001679554 | POPPER & SONS, INC. |