# Deltec, Inc.

- Location (FDA's records): St. Paul, MN
- FDA decisions: 5 (2002–2003): 5 510(k) clearances
- Product codes: FPA (2), MSD (1), LZG (1), MPB (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 10 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtronic Minimed: 3 (https://510kreport.com/company/medtronic-minimed)
- Sims Deltec, Inc.: 1 (https://510kreport.com/company/sims-deltec)

## Firms that cite its devices most
- Smiths Medical MD, Inc.: 1 (https://510kreport.com/company/smiths-medical-md)
- Laboratoires Perouse: 1 (https://510kreport.com/company/laboratoires-perouse)
- Smiths Medical Asd, Inc.: 1 (https://510kreport.com/company/smiths-medical-asd)

## Its most-cited devices
- K021999: Gripper Plus Needle (2002), cited by 2
- K031361: Cadd High-Volume Administration Sets with Flowstop (2003), cited by 1

## Recent decisions
- K031361: Cadd High-Volume Administration Sets with Flowstop (May 23, 2003)
- K030983: Truflow Dual-Lumen Polyurethane Long-Term Straight Dialysis Catheter (12.5 FR X 24 CM) with Tray, Truflow Dual-Lumen Poy (Apr 25, 2003)
- K022221: Truflow Long-Term and Short-Term Dual-Lumen Dialysis Catheters (Jan 30, 2003)
- K020655: Deltec Insulin Infusion Pump and Accessories (Aug 13, 2002)
- K021999: Gripper Plus Needle (Aug 13, 2002)

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