# K895676: Hemostat/Stimulator Probe

- Pathway: 510(k) (Traditional)
- Applicant: Rln Systems, Inc.
- Decided: Dec 8, 1989 after 79 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
No predicates in its family tree.
5 later devices descend from it; 2 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K110712: Drytouch Suction Stimulator Probe (2011), 3 descendants of its own
- 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
- K121931: Nondisposable Stimulating Instruments (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K895676
Methodology: https://510kreport.com/methodology