GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEX— 510(k) K863009

Name: FDA 510(k) clearance K863009
Creator: U.S. Food and Drug Administration
Published: 1986-09-25

Substantially Equivalent

Sds Dental, Inc.

FDA 510(k) clearance K863009 for GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEX, Substantially Equivalent on 1986-09-25. Applicant: Sds Dental, Inc.. Device class: 1.

Clearance details

Applicant: Sds Dental, Inc.
Product code: Code EJP
Device class: Class 1
Regulation: 21 CFR 872.3150
Advisory panel: Dental
Date received: 1986-08-08
Decision date: 1986-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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