Quantimetrix Urine Drugs of Abuse Control

FDA 510(k) K873467 · Quantimetrix Medical Industries

Substantially Equivalent

510(k) numberK873467

Submission

Device name
Quantimetrix Urine Drugs of Abuse Control
Applicant
Quantimetrix Medical Industries
Hawthorne, CA, US
Received
August 28, 1987
Decision date
September 29, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DIF – Drug Mixture Control Materials
Device class
Class I (low risk)
Regulation
21 CFR 862.3280
Specialty
Clinical Toxicology

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More from Roche Diagnostics Corp.

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
K861448Quantimetrix Serum Lipid Control I & II LiquidJJY · Traditional 04/28/1986SE

Questions and answers

When was Quantimetrix Urine Drugs of Abuse Control cleared by the FDA?

Quantimetrix Urine Drugs of Abuse Control (K873467) received a 510(k) decision of Substantially Equivalent on September 29, 1987, 32 days after the submission was received.

What is the product code of K873467?

The FDA product code is DIF – Drug Mixture Control Materials, a Class I (low risk) device regulated under 21 CFR 862.3280.