# Neostar Medical Technologies, Inc.

- Location (FDA's records): King Of Prussia, PA
- FDA decisions: 4 (1995–1996): 4 510(k) clearances
- Product codes: FOZ (2), DYB (1), KOC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- B.Braun Medical, Inc.: 1 (https://510kreport.com/company/b-braun-medical)
- Kendall Healthcare Products Co. Div.Of Tyco Health: 1 (https://510kreport.com/company/kendall-healthcare-products-co-div-of-tyco-health)

## Its most-cited devices
- K941851: Dual Lumen Catheter (DLC) Tray (1995), cited by 2

## Recent decisions
- K960625: Spreadable Sheath Introducer Set (Aug 8, 1996)
- K944660: Acute Central Venous Access Catheter Tray (Mar 13, 1995)
- K941851: Dual Lumen Catheter (DLC) Tray (Mar 13, 1995)
- K944511: Acute Central Venous Access Catheter (Acvac) (Mar 13, 1995)

Source page: https://510kreport.com/company/neostar-medical-technologies