# K981907: V.F.I.-Viscous Fluid Infusion Tubing Set

- Pathway: 510(k) (Traditional)
- Applicant: Peregrine Surgical, Ltd.
- Decided: Aug 4, 1998 after 64 days
- Product code: MRH (Pump, Infusion, Ophthalmic)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Grieshaber & Co. V.L.S. Pack Tubing Set: named in the summary without a submission number

## Indications for use
For pneumatic infusion of silicone oil into the posterior segment.

Source page: https://510kreport.com/device/K981907
Methodology: https://510kreport.com/methodology