Popper Sons Inc

FDA Filings

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.

FDA Filings

Device Company	Device	Date
PMN K911397 POPPER & SONS, INC.	HYPODERMIC NEEDLES, SINGLE LUMEN	1991-05-20
PMN K843830 POPPER & SONS, INC.	J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI	1984-10-26
PMN K843690 POPPER & SONS, INC.	ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE	1984-10-25
PMN K842406 POPPER & SONS, INC.	WESCOTT TYPE BIOPSY NEEDLE	1984-08-09
PMN K841301 POPPER & SONS, INC.	GARDNER TYPE BONE MARROW NEEDLE	1984-06-05
PMN K841300 POPPER & SONS, INC.	ANTRUM NEEDLE-WOLF TYPE	1984-06-05
PMN K841299 POPPER & SONS, INC.	BIERMAN BIOPSY NEEDLE	1984-05-02
PMN K840168 POPPER & SONS, INC.	WESTERMAN-JENSEN BIOPSY NEEDLE	1984-03-12

Related Finance Registrations

NCAGE Code	95388	POPPER & SONS INC.
CAGE Code	95388	POPPER & SONS, INC.
DUNS	001679554	POPPER & SONS, INC.