Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Aqua Medical with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 8, 2025: Aqua Medical RF Vapor Ablation System.
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.
| Aug 8, 2025 | Aqua Medical RF Vapor Ablation SystemK251226 · KNS | 510(k) clearances |
| Dec 12, 2024 | Aqua Medical RF Vapor Ablation SystemK241271 · KNS | 510(k) clearances |
| Dec 17, 2021 | RF Vapor SystemK213627 · KNS | 510(k) clearances |
| May 27, 2021 | Aqua Medical RF Vapor SystemK211282 · KNS | 510(k) clearances |
| Jun 21, 2019 | Aqua Medical RF Vapor SystemK183595 · KNS | 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
