# K953078: Storz DP4101 Basic I/a Pack

- Pathway: 510(k) (Traditional)
- Applicant: Storz Instrument Co.
- Decided: Aug 7, 1995 after 35 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
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K961874: Storz DP5100 Anterior Collection Cassette Pack (1996), 1 descendant of its own
- K990292: I/a (Irrigation/Aspiration) Pack, Posterior Vitrecomy Pack, Anterior Virectomy Pack, Phacoemulsification Pack, Admiinisn (1999), 0 descendants of its own
- K961820: Storz DP4600 Anterior Intraocular Pressure Control Pack (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K953078
Methodology: https://510kreport.com/methodology