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Popper & Sons, Inc.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K911397	HYPODERMIC NEEDLES, SINGLE LUMEN	FCG	1991-05-20	View
510(k)	K843830	J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI	GDM	1984-10-26	View
510(k)	K843690	ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE	GDM	1984-10-25	View
510(k)	K842406	WESCOTT TYPE BIOPSY NEEDLE		1984-08-09	View
510(k)	K841300	ANTRUM NEEDLE-WOLF TYPE		1984-06-05	View
510(k)	K841301	GARDNER TYPE BONE MARROW NEEDLE	GAA	1984-06-05	View
510(k)	K841299	BIERMAN BIOPSY NEEDLE	GDM	1984-05-02	View
510(k)	K840168	WESTERMAN-JENSEN BIOPSY NEEDLE	FCG	1984-03-12	View

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