# K933576: Arthroscope, Disposable

- Pathway: 510(k) (Traditional)
- Applicant: United States Surgical, A Division of Tyco Healthc
- Decided: Apr 21, 1994 after 272 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K140903: Nuvis Arthroscope (2014), 2 descendants of its own
- K191594: Nuvis Battery Arthroscope (2019), 0 descendants of its own
- K152511: Neo - Arthroscope (Rigid) 2.0mm/3.5mm, Outer sheath/ cannula, Outer sheath/ cannula w/ Handle, Trocar for outersheath/ cannula (2016), 0 descendants of its own
- K960805: Arthoscope (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K933576
Methodology: https://510kreport.com/methodology