# K954816: Storz DP4800 Deluxe , Storz DP4801 Basic W/Reflux, DP4801 Basic Posterior Vitrectomy Pack with Variable Port Cutter & RX

- Pathway: 510(k) (Traditional)
- Applicant: Storz Instrument Co.
- Decided: Mar 4, 1996 after 136 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
Longest line of descent: 1 generation back to K953575 (1995). 1 ancestor in all.
2 later devices descend from it; 1 cites 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)
- K953575: Storz MVS-3201 Vitrectomy Probe Pack, Storz Instrument Co. (1995) Summary page 1.

## Most influential descendants
- 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

## Indications for use
The STORZ DP4801, DP4800, and DP4801VP surgical accessory packs contain a vitrectomy probe and attached tubing set to be used in conjunction with the STORZ PREMIERE® or DAISY® Microsurgical Systems in the performance of posterior vitrectomy.

Source page: https://510kreport.com/device/K954816
Methodology: https://510kreport.com/methodology