DIVERSI-KIT— 510(k) K882485

Name: FDA 510(k) clearance K882485
Creator: U.S. Food and Drug Administration
Published: 1988-07-18

Substantially Equivalent

Intl. Cancer Screening Laboratories, Inc.

FDA 510(k) clearance K882485 for DIVERSI-KIT, Substantially Equivalent on 1988-07-18. Applicant: Intl. Cancer Screening Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Intl. Cancer Screening Laboratories, Inc.
Product code: Code LIO
Device class: Class 1
Regulation: 21 CFR 866.2900
Advisory panel: Microbiology
Date received: 1988-06-16
Decision date: 1988-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.