Quantimetrix Serum Lipid Control I & II Liquid

FDA 510(k) K861448 · Quantimetrix Medical Industries

Substantially Equivalent

510(k) numberK861448

Submission

Device name
Quantimetrix Serum Lipid Control I & II Liquid
Applicant
Quantimetrix Medical Industries
Hawthorne, CA, US
Received
March 12, 1986
Decision date
April 28, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJY – Multi-Analyte Controls, All Kinds (Assayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

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More from Aalto Scientific, Ltd.

510(k)DeviceDecision
K895778Quantimetrix Bilirubin CalibratorsJIS · Traditional 11/14/1989SE
K883395Alkphor(Tm) System, Human Serum Alka Phos IsoenzyJJT · Traditional 09/19/1988SE
K883247Lipophor(Tm) Syst, Human Serum Lipoprotein ControlJJY · Traditional 09/13/1988SE
K874302Quantimetrix Total Creatine Kinase ControlJJT · Traditional 02/02/1988SE
K874890Quantimetrix Urine Dipstick ControlJJW · Traditional 01/21/1988SE
K873011Quantimetrix Serum Alcohol Control Level 1 and 2LAS · Traditional 10/29/1987SE
K873467Quantimetrix Urine Drugs of Abuse ControlDIF · Traditional 09/29/1987SE

Questions and answers

When was Quantimetrix Serum Lipid Control I & II Liquid cleared by the FDA?

Quantimetrix Serum Lipid Control I & II Liquid (K861448) received a 510(k) decision of Substantially Equivalent on April 28, 1986, 47 days after the submission was received.

What is the product code of K861448?

The FDA product code is JJY – Multi-Analyte Controls, All Kinds (Assayed), a Class I (low risk) device regulated under 21 CFR 862.1660.