Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of VantiveLabelled by claude-sonnet-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 Cobe Renal Care, Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Sep 25, 1997: GAMBRO FH 22H FIBER HEMOFLTR/PRISMA FH 22H BLOOD TUBING/HEMOFLTR SET.
| Sep 25, 1997 | GAMBRO FH 22H FIBER HEMOFLTR/PRISMA FH 22H BLOOD TUBING/HEMOFLTR SETK955497 · KDL | 510(k) clearances |
| Apr 30, 1997 | COBE CENTRYSYSTEM 14 PES HEMODIALYZERSK955592 · KDI | 510(k) clearances |
| Apr 18, 1997 | GAMBRO POLYFLUX 14, 17, & 21 HEMODIALYZERSK955487 · KDI | 510(k) clearances |
| Feb 10, 1997 | PRISMA CFM (CONTINUOUS FLUID MANAGEMENT SYSTEM)K946279 · KDI | 510(k) clearances |
| Feb 6, 1997 | COBE HEMODYNAMIC RECIRCULATION MONITORK954003 · MQS | 510(k) clearances |
| Aug 14, 1996 | COBE CENTRYSYSTEM 600 HG HEMODIALYZERSK960474 · KDI | 510(k) clearances |
| Jan 29, 1996 | COBE CENTRYSYSTEM CS 200 DIALYZERK944436 · FJI | 510(k) clearances |
| Jan 11, 1996 | GAMBRO HC 14R HEMOCONCENTRATORK951311 · KDI | 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
