Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Mercator MedSystems with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 2, 2021: Bullfrog Micro-Infusion Device.
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 2, 2021 | Bullfrog Micro-Infusion DeviceK210339 · KRA | 510(k) clearances |
| Aug 18, 2016 | Bullfrog Micro-Infusion DeviceK161402 · KRA | 510(k) clearances |
| Apr 15, 2016 | Bullfrog Micro-Infusion DeviceK153501 · KRA | 510(k) clearances |
| Jul 2, 2013 | BLOWFISH TRANSBRONCHIAL MICRO-INFUSION CATHETERK131401 · EOQ | 510(k) clearances |
| Dec 7, 2006 | MERCATOR MICROSYRINGE II INFUSION CATHETERK062752 · KRA | 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
