# K142701: SMD Sr90-1 Radionuclide Brachytherapy Source

- Pathway: 510(k) (Traditional)
- Applicant: Salutaris Medical Devices, Inc.
- Decided: Dec 19, 2014 after 88 days
- Product code: KXK (Source, Brachytherapy, Radionuclide)
- Device class: 2
- Regulation: 21 CFR 892.5730
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K163572: LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source (2017), 1 descendant of its own
- K193602: LV Liberty Vision Model 1 90Yttrium Brachytherapy Source (2020), 0 descendants of its own

## Indications for use
The SMD Sr90-1 Radionuclide Brachytherapy Source (RBS) device is indicated for episcleral brachytherapy of tumors and benign growths. The SMD Sr90-1 RBS device is intended for use within a manual brachytherapy applicator system.

Source page: https://510kreport.com/device/K142701
Methodology: https://510kreport.com/methodology