ACRO RAPID PHENCYCLIDINE URINE TEST, CATALOG PCP001000— 510(k) K060353

Name: FDA 510(k) clearance K060353
Creator: U.S. Food and Drug Administration
Published: 2006-05-03

Substantially Equivalent

Acro Biotech, LLC

FDA 510(k) clearance K060353 for ACRO RAPID PHENCYCLIDINE URINE TEST, CATALOG PCP001000, Substantially Equivalent on 2006-05-03. Applicant: Acro Biotech, LLC. Device class: Unclassified.

Clearance details

Applicant: Acro Biotech, LLC
Product code: Code LCM
Device class: Unclassified
Advisory panel: Unknown
Date received: 2006-02-13
Decision date: 2006-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rancho Cucamonga, CA, US

Download summary PDF View on FDA.gov ↗

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