# K002572: Medtronic PS Medical Channelscope Endoscope, Models 2232-001, 2232-002, 2232-003, 2232-004, 2233-002, 2233-005

- Pathway: 510(k) (Abbreviated)
- Applicant: Medtronic PS Medical
- Decided: Nov 16, 2000 after 90 days
- Product code: GWG (Endoscope, Neurological)
- Device class: 2
- Regulation: 21 CFR 882.1480
- 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
- K190719: Artemis Eye System (2019), 2 descendants of its own
- K201308: Axonpen, Axonmonitor, Axonbox, Tablet (2020), 1 descendant of its own
- K230125: Neuroblade System (2023), 0 descendants of its own
- K014149: Paediscope, Model # P010A and PF011A (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K002572
Methodology: https://510kreport.com/methodology