# K083754: Mini Lap Electrocautery Instruments

- Pathway: 510(k) (Traditional)
- Applicant: Mini Lap Technologies, Inc.
- Decided: Nov 20, 2009 after 338 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K153063: Percuvance  Percutaneous Surgical System (2016), 1 descendant of its own
- K181852: Percuvance Percutaneous Surgical System (2018), 0 descendants of its own
- K172775: MiniLap System with MiniGrip Handle, MiniLap System with ThumbGrip Handle (2018), 0 descendants of its own

## Indications for use
The devices are used to cut and cauterize soft tissue.

Source page: https://510kreport.com/device/K083754
Methodology: https://510kreport.com/methodology