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., part of Avanos MedicalLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Corpak with 24 510(k) clearances. The most recent is a 510(k) clearance dated Jun 26, 1998: CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSIS.
| Jun 26, 1998 | CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSISK964514 · FKO | 510(k) clearances |
| Jul 21, 1997 | CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEMK970178 · KNT | 510(k) clearances |
| Aug 29, 1996 | CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACOREK935512 · KNT | 510(k) clearances |
| Jun 19, 1995 | CORFLO 300 PUMPK944750 · FRN | 510(k) clearances |
| Jun 9, 1995 | CORPAK GASTROSTOMY TUBEK931921 · KNT | 510(k) clearances |
| Jun 17, 1994 | CORPAK ENTERAL PUMPK932847 · FRN | 510(k) clearances |
| Aug 30, 1990 | CORPAK GRASPING FORCEPSK902949 · OCZ | 510(k) clearances |
| Jun 11, 1990 | CORPAK GASTROSTOMY TUBEK901501 · KGC | 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
