FRESENIUS 2008 BSS BEDSIDE DIALYSIS SYSTEM— 510(k) K890329

Substantially Equivalent

Fresenius USA, Inc.

FDA 510(k) clearance K890329 for FRESENIUS 2008 BSS BEDSIDE DIALYSIS SYSTEM, Substantially Equivalent on 1989-05-11. Applicant: Fresenius USA, Inc..

Clearance details

Applicant: Fresenius USA, Inc.
Product code: Code FIL
Advisory panel: Gastroenterology, Urology
Date received: 1989-01-23
Decision date: 1989-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, CA, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.