Stratus(R) Ck-Mb Fluorometric Enzyme Immunoassay

FDA 510(k) K873171 · American Dade

Substantially Equivalent

510(k) numberK873171

Submission

Device name
Stratus(R) Ck-Mb Fluorometric Enzyme Immunoassay
Applicant
American Dade
Santa Ana, CA, US
Received
August 11, 1987
Decision date
September 29, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JHX – Fluorometric Method, Cpk Or Isoenzymes
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1215
Specialty
Clinical Chemistry

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More from Beckman Coulter, Inc.

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K873051Stratus(R) HFSH Fluorometric Enzyme ImmunoassayCGJ · Traditional 10/20/1987SE
K873052Stratus(R) HLH Fluorometric Enzyme ImmunoassayCEP · Traditional 09/14/1987SE
K872789Paramax Urine/Csf CalibratorJIX · Traditional 09/02/1987SE
K872195Data-Fi Dimertest Latex AssayDAP · Traditional 08/06/1987SE
K872196Aqueous Blood Gas/Electrolyte Contr Lev I,Ii & IIIJJS · Traditional 07/31/1987SE
K871972Stratus Ige Fluorometric Enzyme ImmunoassayDGE · Traditional 07/21/1987SE
K871977Dade Moni-Trol Chemistry Control/CalibratorJJY · Traditional 07/09/1987SE
K872050Paramax Cholesterol ReagentLBS · Traditional 07/07/1987SE
K872360Data-Fi Fibrin(Ogen) Degradation Prod.(Fdp)Det SetGHH · Traditional 07/06/1987SE
K870158Stratus Free Thyroxine (FT4) Fluor. Enzyme Immuno.CEC · Traditional 03/19/1987SE

Questions and answers

When was Stratus(R) Ck-Mb Fluorometric Enzyme Immunoassay cleared by the FDA?

Stratus(R) Ck-Mb Fluorometric Enzyme Immunoassay (K873171) received a 510(k) decision of Substantially Equivalent on September 29, 1987, 49 days after the submission was received.

What is the product code of K873171?

The FDA product code is JHX – Fluorometric Method, Cpk Or Isoenzymes, a Class II (moderate risk) device regulated under 21 CFR 862.1215.