Cobe Renal Care, Inc.
Cobe Renal Care, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 1997.
Top product codes for Cobe Renal Care, Inc.
Recent clearances by Cobe Renal Care, Inc.
- K955497 — GAMBRO FH 22H FIBER HEMOFLTR/PRISMA FH 22H BLOOD TUBING/HEMOFLTR SET
- K955592 — COBE CENTRYSYSTEM 14 PES HEMODIALYZERS
- K955487 — GAMBRO POLYFLUX 14, 17, & 21 HEMODIALYZERS
- K946279 — PRISMA CFM (CONTINUOUS FLUID MANAGEMENT SYSTEM)
- K954003 — COBE HEMODYNAMIC RECIRCULATION MONITOR
- K960474 — COBE CENTRYSYSTEM 600 HG HEMODIALYZERS
- K944436 — COBE CENTRYSYSTEM CS 200 DIALYZER
- K951311 — GAMBRO HC 14R HEMOCONCENTRATOR
- K952342 — GAMBRO LUNDIA 94-700 & SIGMA 800 HEMODIALYZERS
- K945746 — GAMBRO LUNDIA 94-500 DIALYZER
- K945747 — GAMBRO LUNDIA 94-600 DIALYZER
- K933883 — GAMBRO FH 66 D HEMOFILTER
- K933681 — GAMBRO LUNDIA PRO 100, 500, 600 DIALYZERS
- K933680 — GAMBRO LUNDIA PRO 200 DIALYZER
Data sourced from openFDA. This site is unofficial and independent of the FDA.