# K062072: Pajunks Disposable Inserts for Handle Instruments and HF Electrodes

- Pathway: 510(k) (Special)
- Applicant: PAJUNK GmbH Medizintechnologie
- Decided: Sep 22, 2006 after 63 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: 2 generations back to K935270 (1994). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033249: Pajunk Modular Handle Instruments, Pajunk GmbH (2004) Summary page 1.

## Most influential descendants
- K151567: ENDOPLUS hand-held laparoscopic instruments (2015), 1 descendant of its own
- K193018: Surgical Direct Hand-held Laparoscopic Instruments (2019), 0 descendants of its own

## Indications for use
Pajunks disposable inserts 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/K062072
Methodology: https://510kreport.com/methodology