# K102275: Thermedx 37-5 Electrocautery Probes, Models MPJ200, MPJ210, MPS220, MPN230, BPH240

- Pathway: 510(k) (Traditional)
- Applicant: Thermedx, LLC
- Decided: Mar 25, 2011 after 226 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: 3 generations back to K910831 (1991). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K994319: Modulap, Atc Technologies, Inc. (2000) Summary page 1.
- K061417: Genicon Disposable Electrosurgical Instrumentation, Model 533-005-910, Genicon (2006) Summary page 1.
- K963765: Stryker Strykeflow Electrocautery Probes, Stryker Endoscopy (1997) Summary page 1.
- K012018: Bicap Coag Bipolar Laparoscopy Probe, Model 006908-910, Acmi Corporation (2002) Summary page 1.

## Cited in the summary but kept off the family tree
- K083623: Carpentier-Mccarthy-Adams Imr Etlogix Annuloplasty Ring, Model 4100, Edwards Lifesciences, LLC (2009). Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Indications for use
The Thermedx 37-5 electrocautery probes are indicated for electrosurgical cutting and coagulation during a variety of urology, gynecology, laparoscopy and general surgery procedures.

Source page: https://510kreport.com/device/K102275
Methodology: https://510kreport.com/methodology