# Menlo Care, Inc.

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 31 (1986–1997): 31 510(k) clearances
- Product codes: FOZ (22), DYB (2), FAD (2), KMK (1), LJS (1), LJE (1), FGE (1)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Luther Medical Products, Inc.: 1 (https://510kreport.com/company/luther-medical-products)

## Recent decisions
- K964447: Picc Catheter/Midline Catheter (Apr 16, 1997)
- K951620: Midmark Midline Catheter (Apr 4, 1996)
- K945521: Centermark (R) Picc Insertion Tray Landmark (R) Midline Catheter Prep Tray (Apr 6, 1995)
- K944968: Landmark Midline Catheter (Mar 29, 1995)
- K950737: Landmark Midline Catheter (Mar 29, 1995)
- K943893: Percutaneous Grainage Catheter (Mar 7, 1995)
- K943143: Biliary Stent (Feb 28, 1995)
- K930048: Safe-Picc Catheter (May 12, 1994)

Source page: https://510kreport.com/company/menlo-care