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 Gabriel Medical with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 27, 1996: INFRA VISION BOUGIE KIT, INFRA VISION ESOPHAGEAL KIT.
| Jun 27, 1996 | INFRA VISION BOUGIE KIT, INFRA VISION ESOPHAGEAL KITK960173 · FAT | 510(k) clearances |
| Feb 7, 1995 | GABRIEL URETERAL ILLUMINATOR SYSTEM IIK945088 · FCS | 510(k) clearances |
| Dec 20, 1994 | INFRA VISION IMAGING SYSTEMK945297 · GCJ | 510(k) clearances |
| May 2, 1994 | GABRIEL URETERAL ILLUMINATOR SYSTEMK940019 · FCS | 510(k) clearances |
| May 9, 1990 | GABRIEL MEDICAL CLS THERMAL RECORDERK901385 · DSF | 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
