# W.E. Leder Enterprises, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1983–1983): 6 510(k) clearances
- Product codes: BSZ (3), CBK (1), CCW (1), DPS (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
- Arco Medic, Ltd.: 1 (https://510kreport.com/company/arco-medic)

## Its most-cited devices
- K831981: Laryngescope (1983), cited by 1

## Recent decisions
- K831877: ARF 850 E (Nov 3, 1983)
- K831981: Laryngescope (Sep 29, 1983)
- K831878: Cardio-Scope Mini Monitor (Sep 29, 1983)
- K830159: Anesthesia Apparatus PH-35 (Mar 9, 1983)
- K830161: Anesthesia Apatatus #D-25 (Mar 9, 1983)
- K830160: Anesthesia Apparatus #FO 20S (Mar 9, 1983)

Source page: https://510kreport.com/company/we-leder-enterprises