# K955093: Aspiration/Coagulation Electrode Ace-311 & Ace-511

- Pathway: 510(k) (Traditional)
- Applicant: Utah Medical Products, Inc.
- Decided: Apr 29, 1996 after 174 days
- Product code: HGI (Electrocautery, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.4120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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) DBL-311 ball electrodes: named in the summary without a submission number
- (no number) DBL-511 ball electrodes: named in the summary without a submission number
- (no number) Valleylab E2505-10FR disposable electrode: named in the summary without a submission number

## Most influential descendants
- K965245: TBD (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K955093
Methodology: https://510kreport.com/methodology