Qbc(R) Centrifugal Hematology Contr/Multi Modified

FDA 510(k) K891907 · R&D Systems, Inc.

Substantially Equivalent

510(k) numberK891907

Submission

Device name
Qbc(R) Centrifugal Hematology Contr/Multi Modified
Applicant
R&D Systems, Inc.
Minneapolis, MN, US
Received
March 27, 1989
Decision date
April 11, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JCN – Control, Cell Counter, Normal And Abnormal
Device class
Class II (moderate risk)
Regulation
21 CFR 864.8625
Specialty
Hematology

Other 510(k)s with product code JCN

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K993825Para Tech Plus ReticsJCN · Traditional Streck Laboratories, Inc.11/30/1999SE
K942209Liquichek HEMATOLOGY-16 Control, Low, Normal and HighJCN · Traditional Bio-Rad06/16/1994SE
K934497Cbc-Stk(Tm) Hematology Control/MultipleJCN · Traditional R&D Systems, Inc.12/06/1993SE
K911582Stak-ChexJCN · Traditional Streck Laboratories, Inc.05/28/1991SE
K902391Cell-Dyn 3000 ControlJCN · Traditional Unipath , Ltd.08/22/1990SE
K902389Tri-Count 16JCN · Traditional Hematronix, Inc.08/22/1990SE
K901875Para 12 PlusJCN · Traditional Streck Laboratories, Inc.05/30/1990SE
K896154Para Tech for Technicon H-1JCN · Traditional Streck Laboratories, Inc.11/09/1989SE
K895373Hematology ControlJCN · Traditional Medical Specialties Intl., Inc.10/06/1989SE
K874386Cbc-Tech(Tm) Hematology Control/MultipleJCN · Traditional R&D Systems, Inc.12/30/1987SE

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Questions and answers

When was Qbc(R) Centrifugal Hematology Contr/Multi Modified cleared by the FDA?

Qbc(R) Centrifugal Hematology Contr/Multi Modified (K891907) received a 510(k) decision of Substantially Equivalent on April 11, 1989, 15 days after the submission was received.

What is the product code of K891907?

The FDA product code is JCN – Control, Cell Counter, Normal And Abnormal, a Class II (moderate risk) device regulated under 21 CFR 864.8625.