Acro Rapid Phencyclidine Urine Test, Catalog PCP001000

FDA 510(k) K060353 · Acro Biotech, LLC

Substantially Equivalent

510(k) numberK060353

Submission

Device name
Acro Rapid Phencyclidine Urine Test, Catalog PCP001000
Applicant
Acro Biotech, LLC
Rancho Cucamonga, CA, US
Received
February 13, 2006
Decision date
May 3, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LCM – Enzyme Immunoassay, Phencyclidine
Device class
Unclassified

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Questions and answers

When was Acro Rapid Phencyclidine Urine Test, Catalog PCP001000 cleared by the FDA?

Acro Rapid Phencyclidine Urine Test, Catalog PCP001000 (K060353) received a 510(k) decision of Substantially Equivalent on May 3, 2006, 79 days after the submission was received.

What is the product code of K060353?

The FDA product code is LCM – Enzyme Immunoassay, Phencyclidine, a Unclassified device.