# K861248: Curapuls 419 Diathermy Unit

- Pathway: 510(k) (Traditional)
- Applicant: Henley Intl.
- Decided: May 30, 1986 after 58 days
- Product code: IMJ (Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat)
- Device class: 2
- Regulation: 21 CFR 890.5290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
63 later devices descend from it; 1 cites it directly.
0 of 64 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
- K022458: Auto*Therm 395, Model ME 395 (2002), 62 descendants of its own
- K083433: Intelect SWD 100, Model 1600; Senior Solutions Shortwave Diathermy, Model 1601 (2009), 61 descendants of its own
- K090221: Reaction System (2009), 54 descendants of its own
- K133837: Viora V-Total (2014), 33 descendants of its own
- K142093: V20 System (2014), 32 descendants of its own

Source page: https://510kreport.com/device/K861248
Methodology: https://510kreport.com/methodology