# K000961: Aaron 900 High Frequency Dessiccator/Handpiece

- Pathway: 510(k) (Special)
- Applicant: Aaron Medical Industries
- Decided: Apr 19, 2000 after 26 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.
17 later devices descend from it; 2 cite it directly.
0 of 18 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
- 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
- K212329: Plasma IQ (2021), 5 descendants of its own
- K201738: SubNovii Advanced Plasma Technology (2020), 5 descendants of its own
- K223222: Plasma IQ (2023), 3 descendants of its own

Source page: https://510kreport.com/device/K000961
Methodology: https://510kreport.com/methodology