# K143203: AveCure Microwave Coagulation-Ablation Generator, AveCure Microwave Large Antenna-Probe, AveCure Microwave Medium Antenna-Probe, AveCure Microwave Small Antenna-Probe, AveCure Microwave Mini Antenna-Probe

- Pathway: 510(k) (Traditional)
- Applicant: Medwaves Incorporated
- Decided: Aug 26, 2015 after 292 days
- Product code: NEY (System, Ablation, Microwave And 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: 10 generations back to K870028 (1987). 55 ancestors in all.
No later device cites it as a predicate yet.
0 of 56 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070356: Medwaves Microwave Coagulation/Ablation System, Medwaves Incorporated (2007) Summary page 4.
- K083537: Modification to Medwaves Microwave Coagulation/Ablation System, Medwaves Incorporated (2009) Summary page 4.
- K122217: Certus 140 2.45GHZ Ablation System, Neuwave Medical, Inc. (2012) Summary page 4.
- K133821: Emprint Ablation System, Covidien, LLC (2014) Summary page 4.

## Indications for use
The MedWaves AveCure™ Ablation System is intended for use in percutaneous, laparoscopic, and intraoperative coagulation-ablation of soft tissue. The MedWaves AveCure™ Ablation System is not intended for use in cardiac procedures.

Source page: https://510kreport.com/device/K143203
Methodology: https://510kreport.com/methodology