# K953575: Storz MVS-3201 Vitrectomy Probe Pack

- Pathway: 510(k) (Traditional)
- Applicant: Storz Instrument Co.
- Decided: Sep 14, 1995 after 45 days
- Product code: HQE (Instrument, Vitreous Aspiration And Cutting, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.4150
- 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; 3 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
- K954816: Storz DP4800 Deluxe , Storz DP4801 Basic W/Reflux, DP4801 Basic Posterior Vitrectomy Pack with Variable Port Cutter & RX (1996), 2 descendants of its own
- K980488: Storz Millennium Microsurgicl System High Speed Vitrectomy System (1998), 1 descendant of its own
- K031404: Dignity Ophthalmic Surgical System (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
- K960003: Storz D7116 Microvit Vitrectomy Cutter Extension (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K953575
Methodology: https://510kreport.com/methodology