Seralyzer CK Reagent Strips

FDA 510(k) K820880 · Miles Laboratories, Inc.

Substantially Equivalent

510(k) numberK820880

Submission

Device name
Seralyzer CK Reagent Strips
Applicant
Miles Laboratories, Inc.
Mchenry, IL, US
Received
March 30, 1982
Decision date
April 16, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CGS – Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1215
Specialty
Clinical Chemistry

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More from Arkray, Inc.

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K880605Labeling Change for Cutter Pureflo Plus IV FilterFPB · Traditional 05/26/1988SE
K874909Micro-Bumintest Reagent TabletsJIR · Traditional 04/28/1988SE
K875079Modified Seralyzer Alt/Sgpt Reag. Strips & ModuleCKA · Traditional 04/05/1988SE
K871835Glucometer QC Blood Meter, Ames Gluco System PrintCGA · Traditional 12/22/1987SE
K872120Seralyzer III Blood Chemistry AnalyzerJJF · Traditional 10/28/1987SE
K873304Clinitek Auto 2000 Reagent Cassette (Leukocytes)LJX · Traditional 09/11/1987SE
K872634Cutter Pureflo Plus IV FilterFPB · Traditional 08/04/1987SE
K870214Modified Saltex Reagent StripsCHK · Traditional 06/29/1987SE
K870752Seralyzer Ldh/Total Bilirubin/Triglycerides StripsCFJ · Traditional 04/14/1987SE
K865053Sera-Tek Microsomal Antibody TestJZO · Traditional 02/18/1987SE

Questions and answers

When was Seralyzer CK Reagent Strips cleared by the FDA?

Seralyzer CK Reagent Strips (K820880) received a 510(k) decision of Substantially Equivalent on April 16, 1982, 17 days after the submission was received.

What is the product code of K820880?

The FDA product code is CGS – Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes, a Class II (moderate risk) device regulated under 21 CFR 862.1215.