# K885005: Microvasive Gold Probe

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corp
- Decided: Feb 1, 1989 after 62 days
- Product code: KNS (Unit, Electrosurgical, Endoscopic (With Or Without Accessories))
- Device class: 2
- Regulation: 21 CFR 876.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 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
- K942301: Microvasive Injection Gold Probe (1994), 6 descendants of its own
- K961349: Injection Gold Probe (1996), 5 descendants of its own
- K110887: Injection Gold Probe Bipolar Electrohemostasis Catheter (2011), 4 descendants of its own
- K133933: Injection Gold Probe Bipolar Electrohemostasis Catheter (2014), 3 descendants of its own
- K171983: Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory (2017), 1 descendant of its own

Source page: https://510kreport.com/device/K885005
Methodology: https://510kreport.com/methodology