Popper & Sons, Inc.

8 FDA 510(k) medical device clearances.

Top product codes for Popper & Sons, Inc.

GDM — General, Plastic Surgery 3 devices
FCG — Gastroenterology, Urology 2 devices
GAA — General, Plastic Surgery 1 device

Recent clearances by Popper & Sons, Inc.

K911397 — HYPODERMIC NEEDLES, SINGLE LUMEN FCG · 1991-05-20
K843830 — J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI GDM · 1984-10-26
K843690 — ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE GDM · 1984-10-25
K842406 — WESCOTT TYPE BIOPSY NEEDLE · 1984-08-09
K841300 — ANTRUM NEEDLE-WOLF TYPE · 1984-06-05
K841301 — GARDNER TYPE BONE MARROW NEEDLE GAA · 1984-06-05
K841299 — BIERMAN BIOPSY NEEDLE GDM · 1984-05-02
K840168 — WESTERMAN-JENSEN BIOPSY NEEDLE FCG · 1984-03-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.