SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET— 510(k) K900991

Name: FDA 510(k) clearance K900991
Creator: U.S. Food and Drug Administration
Published: 1990-05-15

Substantially Equivalent

Tocad America, Inc.

FDA 510(k) clearance K900991 for SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET, Substantially Equivalent on 1990-05-15. Applicant: Tocad America, Inc.. Device class: 1.

Clearance details

Applicant: Tocad America, Inc.
Product code: Code EFS
Device class: Class 1
Regulation: 21 CFR 872.6510
Advisory panel: Dental
Date received: 1990-03-02
Decision date: 1990-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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