# K190251: RecoveryRx

- Pathway: 510(k) (Traditional)
- Applicant: Bioelectronics Corporation
- Decided: Jun 28, 2019 after 141 days
- Product code: ILX (Diathermy, Shortwave, For Use Other Than 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
Longest line of descent: 2 generations back to K903675 (1991). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022404: Actiband, Paw, LLC (2002) Summary page 4.
- K070541: Ivivi Sofpulse, Models 912-M10, ROMA3 and Torino II, Ivivi Technologies, Inc. (2008) Summary page 4.

## Indications for use
Adjunctive treatment of postoperative pain

Source page: https://510kreport.com/device/K190251
Methodology: https://510kreport.com/methodology