Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K173300
›
Descendants
Devices descending from K173300
2 later devices reach ViaTherm BOOST through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K250376
ViVY
Viatherm Therapeutics, LLC
2025
0
—
+1
K223620
Reprieve by RegenesisTM
Regenesis Biomedical, Inc.
2023
0
—