# K893874: Fujitens Iii

- Pathway: 510(k) (Traditional)
- Applicant: Altoona Medical Supply
- Decided: Dec 22, 1989 after 210 days
- Product code: GZQ (Instrument, Dowel Cutting)
- Device class: 2
- Regulation: 21 CFR 882.4275
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 5 cite it directly.
0 of 10 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
- K022731: V Tens Plus (2002), 4 descendants of its own
- K081835: Acticare IC and Tse (2009), 3 descendants of its own
- K161091: STIMPOD NMS460 Nerve Stimulator (2017), 2 descendants of its own
- K252712: STIMPOD NMS460 Nerve Stimulator (2026), 0 descendants of its own
- K213802: StimOnTM Pain Relief System (GM2439) (2022), 0 descendants of its own

Source page: https://510kreport.com/device/K893874
Methodology: https://510kreport.com/methodology