# K010341: Medtronic PS Medical Murphyscope, Models 2125-032, 2125033,2125-042, 2125-043, 2125-157, 2125-158,2125-161 2125-162,,

- Pathway: 510(k) (Abbreviated)
- Applicant: Medtronic PS Medical
- Decided: Apr 20, 2001 after 74 days
- Product code: GWG (Endoscope, Neurological)
- Device class: 2
- Regulation: 21 CFR 882.1480
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Feb 28, 2005 · Not classified · Z-0615-05: Products are mislabeled.
- Feb 28, 2005 · Not classified · Z-0616-05: Products are mislabeled.

Source page: https://510kreport.com/device/K010341
Methodology: https://510kreport.com/methodology