Primus Liquid Calibrator for GHB/A1C Level 1 and Level 2

FDA 510(k) K994045 · Primus Corp.

Substantially Equivalent

510(k) numberK994045

Submission

Device name
Primus Liquid Calibrator for GHB/A1C Level 1 and Level 2
Applicant
Primus Corp.
Kansas City, MO, US
Received
November 29, 1999
Decision date
December 21, 1999
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LCP – Assay, Glycosylated Hemoglobin
Device class
Class II (moderate risk)
Regulation
21 CFR 864.7470
Specialty
Hematology

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K992921Primus Liquid Control for Ghb/Alc Level I and Level IILCP · Traditional 11/12/1999SE
K955283Primus Variant System PVS99GKA · Traditional 03/01/1996SE
K942009Primus Rapid Gel 100 Glycated Hemoglobin AssayLCP · Traditional 09/14/1994SE
K940008Glycated Protein CalibratorsJIS · Traditional 05/09/1994SE
K940142Glycated Protein ControlsJJX · Traditional 04/26/1994SE
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Questions and answers

When was Primus Liquid Calibrator for GHB/A1C Level 1 and Level 2 cleared by the FDA?

Primus Liquid Calibrator for GHB/A1C Level 1 and Level 2 (K994045) received a 510(k) decision of Substantially Equivalent on December 21, 1999, 22 days after the submission was received.

What is the product code of K994045?

The FDA product code is LCP – Assay, Glycosylated Hemoglobin, a Class II (moderate risk) device regulated under 21 CFR 864.7470.