# Loseff Medical Designers, Ltd.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 2 (1980–1980): 2 510(k) clearances
- Product codes: GBA (1), JCX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K802025: Balloon Retention Chest Catheter (Sep 26, 1980)
- K801349: Loseff Balloon Type Self-Retention Wound (Aug 7, 1980)

Source page: https://510kreport.com/company/loseff-medical-designers
