# K003462: Erbe Apc Handle and Applicators, Model 20132-043,20132-031,20132-032,20132-033,20132-034,20132-040,20132-044,20132-045

- Pathway: 510(k) (Abbreviated)
- Applicant: Erbe USA, Inc.
- Decided: Jan 4, 2001 after 58 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
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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K183445: Erbe APCapplicators (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K003462
Methodology: https://510kreport.com/methodology