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 Dravon Medical with 16 510(k) clearances. The most recent is a 510(k) clearance dated Sep 14, 1987: S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSIS.
| Sep 14, 1987 | S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSISK873455 · FJK | 510(k) clearances |
| Apr 21, 1986 | AM-100 I/A AMPACK860770 · HQC | 510(k) clearances |
| Dec 22, 1983 | STEDIFLO INFUSION SETK832739 · LDR | 510(k) clearances |
| Sep 26, 1983 | DRAVON T CLAMPK831842 · KDC | 510(k) clearances |
| Oct 19, 1981 | PERITONEAL DIALYSIS CYCLER SET (8UNIT)K812772 · KDJ | 510(k) clearances |
| Oct 19, 1981 | PERITONEAL DIALYSIS DRAINAGEK812771 · KDJ | 510(k) clearances |
| Aug 31, 1981 | S-610 SHUNT ADAPTOR SETK811851 · KNR | 510(k) clearances |
| Mar 12, 1980 | HEMOSTATIC/TUBE OCCLUDING FORCEPSK800435 · GEN | 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
