# K960262: Coring Morcellator

- Pathway: 510(k) (Traditional)
- Applicant: Cook Urological, Inc.
- Decided: Apr 15, 1996 after 88 days
- Product code: HET (Laparoscope, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1720
- Recalls of this device: none
- 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. The FDA summary names its predicate without a number.
- (no number) Serrated Edged Macro Morcellator (S*E*M*M*-Set): named in the summary without a submission number
- (no number) Birtcher Endoscopic Corkscrew: named in the summary without a submission number

## Indications for use
The Coring Morcellator is used during laparoscopic surgery for the removal of a non-malignant fibroid tumor or other tissue within the peritoneal cavity.

Source page: https://510kreport.com/device/K960262
Methodology: https://510kreport.com/methodology