# K881413: Electro-Cautery Suction Tube

- Pathway: 510(k) (Traditional)
- Applicant: Alto Development Corp.
- Decided: Apr 21, 1988 after 17 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: 2 (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 has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Dec 19, 2013 · Class II · Z-0771-2014: Sterility cannot be guaranteed.
- Dec 19, 2013 · Class II · Z-0770-2014: Sterility cannot be guaranteed.

Source page: https://510kreport.com/device/K881413
Methodology: https://510kreport.com/methodology