# K062047: Adaptable Monopolar Adaptable and/or Retractable Electrodes

- Pathway: 510(k) (Special)
- Applicant: PAJUNK GmbH Medizintechnologie
- Decided: Oct 5, 2006 after 77 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 K935270 (1994). 5 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053282: Adaptable Monopolar Electrodes with Ceramic Tip, Pajunk GmbH (2005). Our reading of the summary gave K063282, FDA’s number for Contiplex Stim Continuous Nerve Block Set (B.Braun Medical, Inc.), decided Jun 20, 2007, after this device. Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “Pajunk's monopolar Ceramic Tip electrodes”.
- K011997: Modular Valve Handles for Adaptable Tubes, Model 1298-XX-XX, 1295-XX-XX, Pajunk GmbH (2001) Summary page 1.
- K033249: Pajunk Modular Handle Instruments, Pajunk GmbH (2004) Summary page 1.

## Most influential descendants
- K190168: Aquas Probes (2019), 0 descendants of its own
- K073498: Laparoscopic and Electrosurgical Instruments and Accessories, Laparoscopy Rudolf System (2008), 0 descendants of its own

## Indications for use
Pajunks HF Electrodes are instruments insulated for optional monopolar coagulation which enable a surgeon to grasp, manipulate, dissect, retrieve, biopsy, cut or coagulate internal tissue or organs while performing laparoscopic procedures.

Source page: https://510kreport.com/device/K062047
Methodology: https://510kreport.com/methodology