Popper & Sons, Inc.
8 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| HYPODERMIC NEEDLES, SINGLE LUMEN (K911397) | Popper & Sons, Inc. | 1991-05-20 |
| J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI (K843830) | Popper & Sons, Inc. | 1984-10-26 |
| ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE (K843690) | Popper & Sons, Inc. | 1984-10-25 |
| WESCOTT TYPE BIOPSY NEEDLE (K842406) | Popper & Sons, Inc. | 1984-08-09 |
| GARDNER TYPE BONE MARROW NEEDLE (K841301) | Popper & Sons, Inc. | 1984-06-05 |
| ANTRUM NEEDLE-WOLF TYPE (K841300) | Popper & Sons, Inc. | 1984-06-05 |
| BIERMAN BIOPSY NEEDLE (K841299) | Popper & Sons, Inc. | 1984-05-02 |
| WESTERMAN-JENSEN BIOPSY NEEDLE (K840168) | Popper & Sons, Inc. | 1984-03-12 |
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Every clearance here is in the API, with alerts when new ones post.