Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Athena GTx, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 26, 2024: WVSM Pro (Series) (500-0030-XX).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 26, 2024 | WVSM Pro (Series) (500-0030-XX)K233354 · MWI | 510(k) clearances |
| Jan 29, 2020 | WVSM (Wireless Vital Signs Monitor) RWC + miniCapK191989 · MWI | 510(k) clearances |
| Mar 14, 2018 | Athena GTX Device Management Suite (ADMS) SoftwareK173203 · MSX | 510(k) clearances |
| Sep 2, 2016 | WiCapK160582 · DQA | 510(k) clearances |
| Jan 28, 2016 | TACVACK153459 · BTA | 510(k) clearances |
| Apr 30, 2013 | WVSM (WIRLESS VITAL SIGNS MONITOR)K130957 · MWI | 510(k) clearances |
| Feb 2, 2012 | MINI-MEDICK113165 · MWI | 510(k) clearances |
| Jul 21, 2010 | WVSM (WIRELESS VITAL SIGNS MONITOR), MODEL 5.0K101674 · MWI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
