# K022856: Bovie Ids-300 High Frequency Electrosurgical Generator

- Pathway: 510(k) (Traditional)
- Applicant: Aaron Medical Industries
- Decided: Feb 10, 2003 after 167 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 K944602 (1995). 2 ancestors in all.
48 later devices descend from it; 5 cite it directly.
0 of 51 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001382: Aaron 2100 High Frequency Electrosurgical Generator, Aaron Medical Industries (2000)
- K944602: Valleylab Force FX, Valleylab, Inc. (1995) Summary page 1.

## Most influential descendants
- K134054: Bovie Ids-310 High Frequency Electrosurgical Generator, Aaron A3350 High Frequency Electrosurgical Generator (2014), 39 descendants of its own
- K161134: Bovie Bantam/PRO Electrosurgical Generator, Bovie DERM 941 Electrosurgical Generator, Bovie DERM 942 Electrosurgical Generator (2016), 14 descendants of its own
- K192813: Plasma IQ (2020), 12 descendants of its own
- K142975: Bovie Ultimate High Frequency Electrosurgical Generator (2014), 12 descendants of its own
- K170188: Bovie J-Plasma Precise Open handpiece & Bovie Ultimate Gen 2 High Frequency Electrosurgical Generator (2017), 11 descendants of its own

## Indications for use
The Bovie IDS 300 High Frequency Electrosurgical Generator is a non-sterile reusable multi-purpose electrosurgical generator that is designed to perform monopolar and bipolar functions in the operating arena.

Source page: https://510kreport.com/device/K022856
Methodology: https://510kreport.com/methodology