# K952204: Conmed/Aspen Labs Coated Laparoscopic Electrosurgical Blades

- Pathway: 510(k) (Traditional)
- Applicant: Conmedcorp
- Decided: May 25, 1995 after 15 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- May 3, 2022 · Class II · Z-1250-2022: Potential for the tip of the electrode to detach during use.

Source page: https://510kreport.com/device/K952204
Methodology: https://510kreport.com/methodology