Statspin Illuminated Micro-Hematocrit Tube Reader

FDA 510(k) K902028 · Norfolk Scientific, Inc.

Substantially Equivalent

510(k) numberK902028

Submission

Device name
Statspin Illuminated Micro-Hematocrit Tube Reader
Applicant
Norfolk Scientific, Inc.
Norwood, MA, US
Received
May 4, 1990
Decision date
June 20, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JPI – Device, Hematocrit Measuring
Device class
Class II (moderate risk)
Regulation
21 CFR 864.6400
Specialty
Hematology

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K950942Crit-Line Hematocrit AlertJPI · Traditional In-Line Diagnostics Corp.03/14/1995SE
K924167Crit-LineJPI · Traditional Noninvasive Medical Technology Corp.05/07/1993SE
K903698Statspin Micro-Hematocrit Reader for 75MM TubesJPI · Traditional Statspin Technologies09/17/1990SE
K870511Chart-Type Micro Hematocrit Tube ReaderJPI · Traditional Norfolk Scientific, Inc.03/16/1987SE
K852516Centifuge, Hematocrit & Microsedimentation CombineJPI · Traditional Whittaker General Medical07/15/1985SE
K852482Microspin Minicentrifuge Item No. 65204/94JPI · Traditional Em Diagnostic Systems, Inc.07/15/1985SE
K850391Plasma Extraction SystemJPI · Traditional Hans J. Brouwers & Assoc.05/10/1985SE
K840767Haemofuge A. Biofuge A. & BJPI · Traditional Heraeus-Christ GmbH04/17/1984SE

More from Heraeus-Christ GmbH

510(k)DeviceDecision
K890669Statspin Hdl-Cholesterol Precipitating Micro TubeLBR · Traditional 03/08/1989SE
K883185Safecrit Plastic Microhematocrit TubesGHY · Traditional 08/18/1988SE
K881254Statspin Disposable Rotor, Product #RD01JQC · Traditional 04/05/1988SE
K870511Chart-Type Micro Hematocrit Tube ReaderJPI · Traditional 03/16/1987SE
K864974General Purpose CentrifugeJQC · Traditional 01/09/1987SE
K860172Qwikspin (TM)JQC · Traditional 02/11/1986SE

Questions and answers

When was Statspin Illuminated Micro-Hematocrit Tube Reader cleared by the FDA?

Statspin Illuminated Micro-Hematocrit Tube Reader (K902028) received a 510(k) decision of Substantially Equivalent on June 20, 1990, 47 days after the submission was received.

What is the product code of K902028?

The FDA product code is JPI – Device, Hematocrit Measuring, a Class II (moderate risk) device regulated under 21 CFR 864.6400.