# K133280: Terumo Surflo I.V. Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Terumo (Philippines) Corporation
- Decided: Jun 12, 2014 after 230 days
- Product code: FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K891087 (1989). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K891087: Terumo Surflo (R) I.V. Catheter, Terumo Medical Corp. (1989) Summary page 2.

## Indications for use
TERUMO®D SURFL0OD I.V. Catheter is inserted into the patient's vascular system for short term use (less than 30 days) to withdraw blood samples, monitor blood pressure, or administer fluids intravenously.

Source page: https://510kreport.com/device/K133280
Methodology: https://510kreport.com/methodology