Company ยท US
Popper & Sons, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1991. Name variants (Inc, Corp, punctuation) are merged.
8510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 20, 1991 | K911397 | HYPODERMIC NEEDLES, SINGLE LUMEN Popper & Sons, Inc. | FCG |
| Oct 26, 1984 | K843830 | J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI Popper & Sons, Inc. | GDM |
| Oct 25, 1984 | K843690 | ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE Popper & Sons, Inc. | GDM |
| Aug 9, 1984 | K842406 | WESCOTT TYPE BIOPSY NEEDLE Popper & Sons, Inc. | |
| Jun 5, 1984 | K841301 | GARDNER TYPE BONE MARROW NEEDLE Popper & Sons, Inc. | GAA |
| Jun 5, 1984 | K841300 | ANTRUM NEEDLE-WOLF TYPE Popper & Sons, Inc. | |
| May 2, 1984 | K841299 | BIERMAN BIOPSY NEEDLE Popper & Sons, Inc. | GDM |
| Mar 12, 1984 | K840168 | WESTERMAN-JENSEN BIOPSY NEEDLE Popper & Sons, Inc. | FCG |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 12, 2008 | Popper & Sons Inc PERFEKTUM TOOMEY EVACUATING SYRINGES, REF/Part # 5047, DESCRIPTION: 30CC LOCK TIP, RX ONLY, NON-STERILE. Manufactured By: Popper & Sons, Inc. New Hyde Park, NY. 11040. Terminated |
FMI | None listed |