# K001382: Aaron 2100 High Frequency Electrosurgical Generator

- Pathway: 510(k) (Traditional)
- Applicant: Aaron Medical Industries
- Decided: Jun 27, 2000 after 56 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
No predicates in its family tree.
49 later devices descend from it; 1 cites it directly.
0 of 50 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K022856: Bovie Ids-300 High Frequency Electrosurgical Generator (2003), 48 descendants of its own
- 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

Source page: https://510kreport.com/device/K001382
Methodology: https://510kreport.com/methodology