# K925903: Laparoscopic 5MM Abc Probe, Modification

- Pathway: 510(k) (Traditional)
- Applicant: Birtcher Medical Systems, Inc.
- Decided: Dec 30, 1992 after 48 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K151229: Abc D-Flex Probe (2016), 0 descendants of its own

## Recalls of this device
- Dec 18, 2008 · Not classified · Z-2281-2010: The internal electrode can protrude in front of ceramic insulator at the tip of the ABC Handpiece used with Conmed Electrosurgical units.
- Dec 18, 2008 · Not classified · Z-2282-2010: The internal electrode can protrude in front of ceramic insulator at the tip of the ABC Handpiece used with Conmed Electrosurgical units.
- Dec 18, 2008 · Not classified · Z-2280-2010: The internal electrode can protrude in front of ceramic insulator at the tip of the ABC Handpiece used with Conmed Electrosurgical units.
- Dec 18, 2008 · Not classified · Z-2279-2010: The internal electrode can protrude in front of ceramic insulator at the tip of the ABC Handpiece used with Conmed Electrosurgical units.

Source page: https://510kreport.com/device/K925903
Methodology: https://510kreport.com/methodology