# K081545: One Series Ultra Cartridge, Model 1VIPR30

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Medical Optics, Inc.
- Decided: Oct 2, 2008 after 122 days
- Product code: MSS (Folders And Injectors, Intraocular Lens (Iol))
- 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
Longest line of descent: 2 generations back to K930320 (1994). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K961242: Amo Phacoflex II Intersection System, Allergan, Inc. (1996) Summary page 5.
- K031692: Safe-Cross Deflecting Catheter, Model C114ND1, Intra Luminal Therapeutics, Inc. (2003) Summary page 5.

## Most influential descendants
- K143434: One Series ULTRA Cartridge, The UNFOLDER Platinum 1 Series (2015), 0 descendants of its own

## Indications for use
Used to fold and assist in inserting TECNIS® 1-Piece intraocular lenses into the eye.

Source page: https://510kreport.com/device/K081545
Methodology: https://510kreport.com/methodology