ULTRASONIC DENTURE CLEANER— 510(k) K881391

Name: FDA 510(k) clearance K881391
Creator: U.S. Food and Drug Administration
Published: 1988-08-26

Substantially Equivalent

Tatung Company of America, Inc.

FDA 510(k) clearance K881391 for ULTRASONIC DENTURE CLEANER, Substantially Equivalent on 1988-08-26. Applicant: Tatung Company of America, Inc.. Device class: 1.

Clearance details

Applicant: Tatung Company of America, Inc.
Product code: Code JER
Device class: Class 1
Regulation: 21 CFR 872.3530
Advisory panel: Dental
Date received: 1988-04-04
Decision date: 1988-08-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Beach, CA, 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.