Quickscreen Methamphetamine Test, Models 9045, 9046, Quickscreen Pro Multi Drug Screening Test, Model 9225

FDA 510(k) K000447 · Phamatech

Substantially Equivalent

510(k) numberK000447

Submission

Device name
Quickscreen Methamphetamine Test, Models 9045, 9046, Quickscreen Pro Multi Drug Screening Test, Model 9225
Applicant
Phamatech
San Diego, CA, US
Received
February 10, 2000
Decision date
March 7, 2000
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LAF – Gas Chromatography, Methamphetamine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3610
Specialty
Clinical Toxicology

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More from Lin-Zhi International, Inc.

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K070098Quickscreen Barbiturate 300 Screening Test, Models 9019, 9018; Multi Drug Screening…DIS · Traditional 12/07/2007SE
K070009At Home Drug Test Models, 9308T and 9308XDIS · Traditional 12/07/2007SE
K043599Moments Menopause Check, Model 9113CGJ · Special 02/25/2005SE
K043051Quickscreen Oxycodone Test, Models 9120, 9120T, 9120X and 9121DJG · Traditional 02/07/2005SE
K043167Phamatech Quickscreen Benzodiazepines Test, Models 9025, 9026, 9027T, 9153T and 9195XJXM · Special 12/29/2004SE
K041578Quickscreen, Models 9177X and 9178XLCM · Special 09/10/2004SE
K040575Pharmatech Menopause Check, Models 9111 and 9112CGJ · Traditional 05/20/2004SE

Questions and answers

When was Quickscreen Methamphetamine Test, Models 9045, 9046, Quickscreen Pro Multi Drug Screening Test, Model 9225 cleared by the FDA?

Quickscreen Methamphetamine Test, Models 9045, 9046, Quickscreen Pro Multi Drug Screening Test, Model 9225 (K000447) received a 510(k) decision of Substantially Equivalent on March 7, 2000, 26 days after the submission was received.

What is the product code of K000447?

The FDA product code is LAF – Gas Chromatography, Methamphetamine, a Class II (moderate risk) device regulated under 21 CFR 862.3610.