CYTOBRUSH— 510(k) K890706

Name: FDA 510(k) clearance K890706
Creator: U.S. Food and Drug Administration
Published: 1989-04-25

Substantially Equivalent

Laboratoire Ccd C/O Washington Regulatory Services

FDA 510(k) clearance K890706 for CYTOBRUSH, Substantially Equivalent on 1989-04-25. Applicant: Laboratoire Ccd C/O Washington Regulatory Services. Device class: 2.

Clearance details

Applicant: Laboratoire Ccd C/O Washington Regulatory Services
Product code: Code HHT
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1989-02-10
Decision date: 1989-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ringoes, NJ, 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.