# K930320: Amo Phacoflex Inserter, Foldable Iol Insert Instr

- Pathway: 510(k) (Traditional)
- Applicant: Allergan Medical Optics
- Decided: Apr 7, 1994 after 440 days
- Product code: KYB (Lens, Guide, Intraocular)
- Device class: 1
- Regulation: 21 CFR 886.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
32 later devices descend from it; 1 cites it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K961242: Amo Phacoflex II Intersection System (1996), 31 descendants of its own
- K040837: Multiject Injector and Microglide Cartridge (2004), 25 descendants of its own
- K070669: Iol Injector Set (2007), 19 descendants of its own
- K092023: Naviject SUB2-1P, Model: LP604430 (2009), 18 descendants of its own
- K113852: Bausch & Lomb Iol Injector (2012), 12 descendants of its own

Source page: https://510kreport.com/device/K930320
Methodology: https://510kreport.com/methodology