# K083428: F7244, F7255, F7266, F7277, F7288, F7233, F7234 Series of Battery-Powered Cautery

- Pathway: 510(k) (Traditional)
- Applicant: Fiab Spa
- Decided: Sep 1, 2009 after 286 days
- Product code: HQP (Unit, Cautery, Thermal, Battery-Powered)
- Device class: 2
- Regulation: 21 CFR 886.4115
- 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) AARON AA04 battery powered cautery: named in the summary without a submission number

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

Source page: https://510kreport.com/device/K083428
Methodology: https://510kreport.com/methodology