# K971275: Mill-Rose Disposable Polypectomy Snare

- Pathway: 510(k) (Traditional)
- Applicant: Mill-Rose Laboratory
- Decided: May 23, 1997 after 46 days
- Product code: FDI (Snare, Flexible)
- Device class: 2
- Regulation: 21 CFR 876.4300
- 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 K792343 (1979). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K912254: Cox Diaposable Polypectomy Snare, Cox Medical Ent., Inc. (1991) Summary page 1.
- K792343: Diathermic Snare (Cresent Type), Mill-Rose Laboratory (1979) Summary page 1.
- K951600: Mill-Rose Rotatable Polypectomy Snare, Mill-Rose Laboratory (1995) Summary page 1.

## Indications for use
The intended use of this device is to electro surgically remove GIL tract -polyps - - - through the channel of an endoscope.

Source page: https://510kreport.com/device/K971275
Methodology: https://510kreport.com/methodology