Fluid, Rhemox-Hb Lysing

FDA 510(k) K790030 · Sysmex Corp.

Substantially Equivalent

510(k) numberK790030

Submission

Device name
Fluid, Rhemox-Hb Lysing
Applicant
Sysmex Corp.
Mchenry, IL, US
Received
January 3, 1979
Decision date
February 8, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GKR – System, Hemoglobin, Automated
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5620
Specialty
Hematology

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K090093Stanbio Laboratory Hemopoint H2 DM Hemoglobin Measurement SystemGKR · Special Stanbio Laboratory06/10/2009SE

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Questions and answers

When was Fluid, Rhemox-Hb Lysing cleared by the FDA?

Fluid, Rhemox-Hb Lysing (K790030) received a 510(k) decision of Substantially Equivalent on February 8, 1979, 36 days after the submission was received.

What is the product code of K790030?

The FDA product code is GKR – System, Hemoglobin, Automated, a Class II (moderate risk) device regulated under 21 CFR 864.5620.