# K974138: Rocket Electrode

- Pathway: 510(k) (Traditional)
- Applicant: A & A Medical, Inc.
- Decided: Jan 30, 1998 after 88 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.
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) Electrodes (Blade, Ball, Needle, Square and Loop) from Aaron Medical Industries: named in the summary without a submission number

## Indications for use
Rocket Electrode is to be used as a gynecologic electrocautery device for tissue excision. It is designed to destroy tissue with high temperatures by tissue contact with an electrically heated probe. This is to excise cervical lesions, perform biopsies, or treat chronic cervititis under direct visual observation

Source page: https://510kreport.com/device/K974138
Methodology: https://510kreport.com/methodology