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 4 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Medcomp with 56 510(k) clearances. The most recent is a 510(k) clearance dated Dec 15, 2017: ArchFlo CT Midline.
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.
| Dec 15, 2017 | ArchFlo CT MidlineK171483 · PND | 510(k) clearances |
| Nov 16, 2017 | Symetrex Long Term Hemodialysis CatheterK171618 · MSD | 510(k) clearances |
| Oct 26, 2017 | Celerity ECG Cable Accessory PackK171931 · LJS | 510(k) clearances |
| Jul 18, 2017 | 20G x 5/8 Pro-Lock CT Safety Infusion SetK171333 · PTI | 510(k) clearances |
| Jun 1, 2017 | Medcomp Vessel DilatorK162389 · DRE | 510(k) clearances |
| Apr 26, 2017 | Pro-Lock CT Safety Infusion SetK162271 · PTI | 510(k) clearances |
| Mar 15, 2016 | Dignity Dual PortK153238 · LJT | 510(k) clearances |
| Feb 12, 2016 | PTFE Super Sheath Introducer 2.1K153246 · DYB | 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
