# K110712: Drytouch Suction Stimulator Probe

- Pathway: 510(k) (Traditional)
- Applicant: Neurovision Medical Products, Inc.
- Decided: Jun 28, 2011 after 106 days
- Product code: ETN (Stimulator, Nerve)
- Device class: 2
- Regulation: 21 CFR 874.1820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K980148 (1998). 12 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K895676: Hemostat/Stimulator Probe, Rln Systems, Inc. (1989) Summary page 1.
- K090838: Stimulus/Dissection Instruments, Axon Systems, Inc. (2009) Summary page 1.
- (no number) Frazier Suction Coagulator (part #23-5001): named in the summary without a submission number

## Most influential descendants
- K133348: Stim Probe (2014), 1 descendant of its own
- K212164: Mapping Suction Probe (2022), 0 descendants of its own
- K152769: Fremap Electrode (2016), 0 descendants of its own

## Indications for use
The Suction Stimulator Probe is a dedicated manual surgical instrument that allows the surgeon to clear secretions and test surgical tissue with nerve stimulation at the same time and with the same instrument. It is intended for use only by a licensed physician and in conjunction with the Neurovision SE (Nerveina) Nerve locator Monitor System.

Source page: https://510kreport.com/device/K110712
Methodology: https://510kreport.com/methodology