Popper & Sons, Inc.
Popper & Sons, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1991.
Top product codes for Popper & Sons, Inc.
Recent clearances by Popper & Sons, Inc.
- K911397 — HYPODERMIC NEEDLES, SINGLE LUMEN
- K843830 — J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI
- K843690 — ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE
- K842406 — WESCOTT TYPE BIOPSY NEEDLE
- K841300 — ANTRUM NEEDLE-WOLF TYPE
- K841301 — GARDNER TYPE BONE MARROW NEEDLE
- K841299 — BIERMAN BIOPSY NEEDLE
- K840168 — WESTERMAN-JENSEN BIOPSY NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.