# K011189: Viaduct Microendoscope and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Acueity, Inc.
- Decided: Jul 16, 2001 after 89 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
43 later devices descend from it; 6 cite it directly.
0 of 44 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
- K020310: Davlite Microendoscope & Accessories (2002), 37 descendants of its own
- K040604: Innervue Diagnostic Scope System (2004), 31 descendants of its own
- K072879: Innervue Diagnostic Scope System (2008), 30 descendants of its own
- K082293: Surgview Integrated Visualization System (2008), 21 descendants of its own
- K093717: C-Mor Visualization Device (2010), 16 descendants of its own

Source page: https://510kreport.com/device/K011189
Methodology: https://510kreport.com/methodology