# K980797: Peregrine Fiber Optic Multi-Function Manipulator

- Pathway: 510(k) (Traditional)
- Applicant: Peregrine Surgical, Ltd.
- Decided: May 19, 1998 after 78 days
- Product code: MPA (Endoilluminator)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
12 later devices descend from it; 2 cite it directly.
0 of 13 devices 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. 3-Function Manipulator: named in the summary without a submission number

## Most influential descendants
- K024061: Peregrine Straight Laser Probe, Model PD6000.00 (2003), 11 descendants of its own
- K031023: Peregrine Illuminating Laser Probe Model PD600.10 (2003), 6 descendants of its own
- K122997: 23GA Curved Illuminating Laser Probe (2013), 4 descendants of its own
- K151604: 23ga Chandelier Illuminator, 25ga Chandelier Illuminator (2015), 2 descendants of its own
- K213467: EVA NEXUS Ophthalmic Surgical System (2022), 1 descendant of its own

## Indications for use
For lllumination, coagulation, irrigation/aspiration, and tissue manipulation during ophthalmic surgery.

Source page: https://510kreport.com/device/K980797
Methodology: https://510kreport.com/methodology