# K914883: Circon Acmi Gen Surg Instru for Mini Invasive Surg

- Pathway: 510(k) (Traditional)
- Applicant: Circon Video
- Decided: Jan 15, 1993 after 443 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.
5 later devices descend from it; 3 cite it directly.
0 of 6 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
- K062337: Modular Laparoscopy Accessories, Handle; Sissors (Straight and Curved); Grasper (Aggressive, Allis, Ataumatic; Dissector (2006), 1 descendant of its own
- K014158: Endoscopic Camera TC804/C4 (2002), 1 descendant of its own
- K081431: Meg Laparoscopic Electrodes (2008), 0 descendants of its own
- K032544: VP-1000; Med Cam 100; VP-3000A; Med Cam 300 (2003), 0 descendants of its own
- K991416: Endoscopic Camera (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K914883
Methodology: https://510kreport.com/methodology