COUPLING DEVICE FOR DENTAL PROSTHESIS— 510(k) K950259

Name: FDA 510(k) clearance K950259
Creator: U.S. Food and Drug Administration
Published: 1996-12-06

Substantially Equivalent

Dr. Joseph E. Grasso, D.D.S.

FDA 510(k) clearance K950259 for COUPLING DEVICE FOR DENTAL PROSTHESIS, Substantially Equivalent on 1996-12-06. Applicant: Dr. Joseph E. Grasso, D.D.S.. Device class: 1.

Clearance details

Applicant: Dr. Joseph E. Grasso, D.D.S.
Product code: Code EGG
Device class: Class 1
Regulation: 21 CFR 872.3165
Advisory panel: Dental
Date received: 1995-01-23
Decision date: 1996-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Simsbury, CT, US

Download summary PDF View on FDA.gov ↗

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