Ics Pab Prealbumin Reagent Test Kit

FDA 510(k) K854811 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK854811

Submission

Device name
Ics Pab Prealbumin Reagent Test Kit
Applicant
Beckman Instruments, Inc.
Fullerton, CA, US
Received
December 3, 1985
Decision date
January 24, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DDS – Prealbumin, Fitc, Antigen, Antiserum, Control
Device class
Class I (low risk)
Regulation
21 CFR 866.5060
Specialty
Immunology

Other 510(k)s with product code DDS

510(k)DeviceApplicantDecision
K972812Raichem Prealbumin SpiaDDS · Traditional Hemagen Diagnostics, Inc.08/28/1997SE
K964781Immage Immunochemistry System Prealbumin (Pab) ReagentDDS · Traditional Beckman Instruments, Inc.05/09/1997SE
K934966SPQ Pal Control Level IIDDS · Traditional Incstar Corp.01/11/1994SE

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K980173Access Total BHCG Reagents on the Access Immunoassay Analyzer; 33500, 33505JHI · Traditional 03/18/1998SE
K974816Access(R) Psa Reagents on the Access(R) Immunoassay Analyzer 33220, 33225, 33229LTJ · Traditional 02/20/1998SE
K974564Immage Immunochemistry System ALPHA-2-MACROGLOBULIN ReagentDEB · Traditional 02/17/1998SE
K974110Immage Immunochemistry System Antithrombin III (AT3) ReagentJBQ · Traditional 12/24/1997SE
K974452Vigil Lipid ControlJJY · Traditional 12/17/1997SE
K973932Beckman Calibrator 2 (CAL2)JIX · Traditional 12/15/1997SE

Questions and answers

When was Ics Pab Prealbumin Reagent Test Kit cleared by the FDA?

Ics Pab Prealbumin Reagent Test Kit (K854811) received a 510(k) decision of Substantially Equivalent on January 24, 1986, 52 days after the submission was received.

What is the product code of K854811?

The FDA product code is DDS – Prealbumin, Fitc, Antigen, Antiserum, Control, a Class I (low risk) device regulated under 21 CFR 866.5060.