# K191947: VASOVIEW HEMOPRO Extension Cable, VASOVIEW HEMOPRO 2 Extension Cable, Bipolar Extension Cable, Fixed Distance, Active Return Cord

- Pathway: 510(k) (Traditional)
- Applicant: Maquet Cardiovascular, LLC
- Decided: Sep 17, 2019 after 57 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
Longest line of descent: 6 generations back to K945975 (1994). 19 ancestors in all.
No later device cites it as a predicate yet.
3 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K153194: VASOVIEW HemoPro Endoscopic Vessel Harvesting System, Maquet Cardiovascular, LLC (2016) Summary page 4.
- K101274: Vasoview Hemopro 2 Endoscopic Vessel Harvesting System, Maquet Cardiovascular, LLC (2010) Summary page 4.
- K091733: Vasoview 6 Pro Endoscopic Vessel Harvesting System, Model VH-2500, Maquet Cardiovascular, LLC (2009) Summary page 4.

## Indications for use
The subject Cables (VASOVIEW HEMOPRO Extension Cable, VASOVIEW HEMOPRO 2 Extension Cable, Bipolar Extension Cable, Fixed Distance and Active Return Cord) are accessories to the VASOVIEW Endoscopic Vessel Harvesting System. They are supplied non-sterile and must be sterilized prior to each.

Source page: https://510kreport.com/device/K191947
Methodology: https://510kreport.com/methodology