KOLYNOS DENTAL FLOSS— 510(k) K882571

Name: FDA 510(k) clearance K882571
Creator: U.S. Food and Drug Administration
Published: 1988-10-12

Substantially Equivalent

Whitehall Laboratories, Inc.

FDA 510(k) clearance K882571 for KOLYNOS DENTAL FLOSS, Substantially Equivalent on 1988-10-12. Applicant: Whitehall Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Whitehall Laboratories, Inc.
Product code: Code JES
Device class: Class 1
Regulation: 21 CFR 872.6390
Advisory panel: Dental
Date received: 1988-06-22
Decision date: 1988-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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