REPGREEN ULTRAFILTRATION MONITOR— 510(k) K790824

Substantially Equivalent

Cyberex Corp.

FDA 510(k) clearance K790824 for REPGREEN ULTRAFILTRATION MONITOR, Substantially Equivalent on 1979-06-27. Applicant: Cyberex Corp.. Device class: 2.

Clearance details

Applicant: Cyberex Corp.
Product code: Code FIL
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1979-05-01
Decision date: 1979-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FIL

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K901038 — SPS 550-IPS (INTEGRATED PATIENT STATION)1990-04-19
K890329 — FRESENIUS 2008 BSS BEDSIDE DIALYSIS SYSTEM1989-05-11
K781633 — ULTRAFILTRATION SCALE1978-12-07
K771875 — ULTRAFILTRATION MONITOR 5M90341977-11-30

More clearances from Cyberex Corp.

K810837 — CYBER 80 HEMODIALYZER1981-05-05
K802478 — CYBER 120 HEMODIALYZER1981-03-20
K801377 — CYBER 120 HEMODIALYZER1980-08-27

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