# K071103: Habib Hexablate

- Pathway: 510(k) (Traditional)
- Applicant: Emcision, Ltd.
- Decided: Jun 27, 2007 after 69 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: 1 generation back to K051420 (2005). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051420: Habib 4X, Emcision, Ltd. (2005) Summary page 1.

## Most influential descendants
- K080717: Habib Hexablate 10 (2008), 0 descendants of its own
- K073687: Habib Laparoscopic Hexablate (2008), 0 descendants of its own

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

Source page: https://510kreport.com/device/K071103
Methodology: https://510kreport.com/methodology