# Popper & Sons, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1984–1991): 8 510(k) clearances
- Product codes: GDM (3), FCG (2), GAA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Bioaccess, Inc.: 1 (https://510kreport.com/company/bioaccess)

## Its most-cited devices
- K843830: J -Jamshidi Type-Bone Marrow Biopsy/Aspi (1984), cited by 1

## Recent decisions
- K911397: Hypodermic Needles, Single Lumen (May 20, 1991)
- K843830: J -Jamshidi Type-Bone Marrow Biopsy/Aspi (Oct 26, 1984)
- K843690: Illinois Sternum/Iliac Aspiration Needle (Oct 25, 1984)
- K842406: Wescott Type Biopsy Needle (Aug 9, 1984)
- K841300: Antrum Needle-Wolf Type (Jun 5, 1984)
- K841301: Gardner Type Bone Marrow Needle (Jun 5, 1984)
- K841299: Bierman Biopsy Needle (May 2, 1984)
- K840168: Westerman-Jensen Biopsy Needle (Mar 12, 1984)

Source page: https://510kreport.com/company/popper-sons