# K070877: Endocervical Electrode # 2

- Pathway: 510(k) (Traditional)
- Applicant: Modern Medical Equipment Mfg., Ltd.
- Decided: Jul 27, 2007 after 120 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
Longest line of descent: 1 generation back to K061651 (2006). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061651: Fischer Cone Biopsy Excisor, Models 900-150, 151, 152, 154, 155, 157 and 158, Apple Medical Corp. (2006) Summary page 2.

## Indications for use
Endocervical Hysterectomy Electrode is indicated for treatment of following Condition 1. Excision of inner cervix during supracervical hysterectomy.

Source page: https://510kreport.com/device/K070877
Methodology: https://510kreport.com/methodology