QBC(R) CENTRIFUGAL HEMATOLOGY CONTR/MULTI MODIFIED— 510(k) K891907

Name: FDA 510(k) clearance K891907
Creator: U.S. Food and Drug Administration
Published: 1989-04-11

Substantially Equivalent

R&D Systems, Inc.

FDA 510(k) clearance K891907 for QBC(R) CENTRIFUGAL HEMATOLOGY CONTR/MULTI MODIFIED, Substantially Equivalent on 1989-04-11. Applicant: R&D Systems, Inc.. Device class: 2.

Clearance details

Applicant: R&D Systems, Inc.
Product code: Code JCN
Device class: Class 2
Regulation: 21 CFR 864.8625
Advisory panel: Hematology
Date received: 1989-03-27
Decision date: 1989-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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K934497 — CBC-STK(TM) HEMATOLOGY CONTROL/MULTIPLE1993-12-06
K911582 — STAK-CHEX1991-05-28
K902389 — TRI-COUNT 161990-08-22

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