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 13, 2026, FDA's public records list Vitaid with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 30, 2005: PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBES.
| Date | Record | Source |
|---|---|---|
| Jun 30, 2005 | PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBESK050803 · BTR | 510(k) clearances |
| Nov 2, 1993 | WIRE REINFORCED ENDOTRACHEAL TUBEK932647 · BTR | 510(k) clearances |
| Jun 27, 1990 | SELFCATHK901738 · KOD | 510(k) clearances |
| Apr 25, 1990 | PHYCON ALL SILICONE BALLOON CATHETERK894883 · EZL | 510(k) clearances |
| Nov 21, 1989 | AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMPK894794 · KPM | 510(k) clearances |
| Oct 13, 1989 | LASER SHIELDING TUBEK894669 · BTR | 510(k) clearances |
| Sep 29, 1989 | UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MMK894337 · CBI | 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
