# K151229: Abc D-Flex Probe

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Corporation
- Decided: Jun 2, 2016 after 392 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: 1 generation back to K925903 (1992). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K925903: Laparoscopic 5MM Abc Probe, Modification, Birtcher Medical Systems, Inc. (1992) Summary page 4.

## Indications for use
The CONMED ABC D-Flex Probes are intended for use with a CONMED ABC Generator for delivery of argon gas and electrosurgical current for non-contact ablation and hemostasis at the operative site. The ABC D-Flex Probes are indicated for use during general, urological, and gynecological laparoscopic surgical procedures when manipulated by CONMED manual laparoscopic graspers or similar manual instruments.

Source page: https://510kreport.com/device/K151229
Methodology: https://510kreport.com/methodology