# K960414: Synergist Power Pack

- Pathway: 510(k) (Traditional)
- Applicant: Chiron Vision Corp.
- Decided: Apr 24, 1996 after 86 days
- Product code: HQC (Unit, Phacofragmentation)
- Device class: 2
- Regulation: 21 CFR 886.4670
- 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 K925631 (1993). 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)
- K925631: Phacotron Gold Multifunction Ultrasonic Handpiece, Chiron Intraoptics (1993) Summary page 1.

## Indications for use
The Synergist™ Power Pack is intended for use in cataract surgery or other ophthalmic surgical procedures where precision surgical tissue removal 1s required.

Source page: https://510kreport.com/device/K960414
Methodology: https://510kreport.com/methodology