# K073687: Habib Laparoscopic Hexablate

- Pathway: 510(k) (Traditional)
- Applicant: Emcision, Ltd.
- Decided: Jan 9, 2008 after 12 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K984552 (1999). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071103: Habib Hexablate, Emcision, Ltd. (2007)
- K062935: Habib 4X Laparoscopic, Rita Medical Systems (2006) Summary page 1.

## Indications for use
The Habib Laparoscopic Hexablate is intended to be used to assist in coagulation of tissue during laparoscopic intraoperative surgical procedures

Source page: https://510kreport.com/device/K073687
Methodology: https://510kreport.com/methodology