SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL)— 510(k) K893800

Name: FDA 510(k) clearance K893800
Creator: U.S. Food and Drug Administration
Published: 1989-12-20

Substantially Equivalent

Deringer-Ney, Inc.

FDA 510(k) clearance K893800 for SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL), Substantially Equivalent on 1989-12-20. Applicant: Deringer-Ney, Inc.. Device class: 2.

Clearance details

Applicant: Deringer-Ney, Inc.
Product code: Code EJT
Device class: Class 2
Regulation: 21 CFR 872.3060
Advisory panel: Dental
Date received: 1989-05-22
Decision date: 1989-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bloomfield, CT, US

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