# K882240: Storz Univ Irrigat/Aspira & Phacoemulsifcation Pac

- Pathway: 510(k) (Traditional)
- Applicant: Storz Instrument Co.
- Decided: Jul 29, 1988 after 63 days
- Product code: GDM (Needle, Aspiration And Injection, Reusable)
- Device class: 1
- Regulation: 21 CFR 878.4800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K955901: Storz DP4310DELUXE Phaco Pack Without Reflux (1996), 4 descendants of its own
- K980100: Storz DP4210 Venturi Economy Anterior Pack and DP5000 Asc  Daypack (1998), 1 descendant of its own
- K961831: Storz DP5200 Irrigation Addministration Set Pack (1996), 1 descendant of its own
- K033653: Venturi Phaco Pack (2003), 0 descendants of its own
- K990292: I/a (Irrigation/Aspiration) Pack, Posterior Vitrecomy Pack, Anterior Virectomy Pack, Phacoemulsification Pack, Admiinisn (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K882240
Methodology: https://510kreport.com/methodology