HYDRODENT ANTIPLAQUE SYSTEM— 510(k) K890600

Unknown

Hydrodent Laboratories, Inc.

FDA 510(k) clearance K890600 for HYDRODENT ANTIPLAQUE SYSTEM, Unknown on 1989-05-05. Applicant: Hydrodent Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Hydrodent Laboratories, Inc.
Product code: Code EFS
Device class: Class 1
Regulation: 21 CFR 872.6510
Advisory panel: Dental
Date received: 1989-02-06
Decision date: 1989-05-05
Decision: Unknown
Clearance type: Traditional
Location: Miami, FL, 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.