# K100333: Fiab Spa, Models F7244, F7233, F7234, F7277

- Pathway: 510(k) (Traditional)
- Applicant: Fiab Spa
- Decided: Jun 21, 2010 after 136 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 K945492 (1995). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K945492: High Temperature Cautery, Aaron Medical Industries (1995) Summary page 1.
- K945759: High Temperature Cautery 5 Loop, Aaron Medical Industries (1995) Summary page 1.

## Indications for use
Cauterisation of tissues and capillary vessels during operations. No high frequency generator is required.

Source page: https://510kreport.com/device/K100333
Methodology: https://510kreport.com/methodology