CYTEX ONE AND CYTEX TWO— 510(k) K890283

Name: FDA 510(k) clearance K890283
Creator: U.S. Food and Drug Administration
Published: 1989-03-16

Substantially Equivalent

Anderson Winn Paper Co.

FDA 510(k) clearance K890283 for CYTEX ONE AND CYTEX TWO, Substantially Equivalent on 1989-03-16. Applicant: Anderson Winn Paper Co.. Device class: 2.

Clearance details

Applicant: Anderson Winn Paper Co.
Product code: Code HHT
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1989-01-19
Decision date: 1989-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burbank, CA, US

Download summary PDF View on FDA.gov ↗

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