INTRAORAL VIDEO SCOPE AND WINDOW TUBE— 510(k) K951019

Name: FDA 510(k) clearance K951019
Creator: U.S. Food and Drug Administration
Published: 1995-05-10

Substantially Equivalent

Cuda Products Co.

FDA 510(k) clearance K951019 for INTRAORAL VIDEO SCOPE AND WINDOW TUBE, Substantially Equivalent on 1995-05-10. Applicant: Cuda Products Co.. Device class: 1.

Clearance details

Applicant: Cuda Products Co.
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1995-03-07
Decision date: 1995-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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