PRECAPSULED DENTAL AMALGAM— 510(k) K822610

Name: FDA 510(k) clearance K822610
Creator: U.S. Food and Drug Administration
Published: 1982-09-14

Substantially Equivalent

Syntex Dental Products, Inc.

FDA 510(k) clearance K822610 for PRECAPSULED DENTAL AMALGAM, Substantially Equivalent on 1982-09-14. Applicant: Syntex Dental Products, Inc.. Device class: 1.

Clearance details

Applicant: Syntex Dental Products, Inc.
Product code: Code DZS
Device class: Class 1
Regulation: 21 CFR 872.3110
Advisory panel: Dental
Date received: 1982-08-30
Decision date: 1982-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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