# The Ludlow Company LP

- Location (FDA's records): Chicopee, MA
- FDA decisions: 3 (2001–2002): 3 510(k) clearances
- Product codes: FRP (1), DRO (1), MUI (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: 8 (4 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K021132: Uni-Patch Ultrasound Coupling Gel (May 15, 2002)
- K012218: Ludlow Gradient Edge Adult & Pediatric Multifunctional Electrodes (Oct 12, 2001)
- K003511: Kendall-LTP Turner Save-a-Line (Jan 24, 2001)

Source page: https://510kreport.com/company/ludlow