REGENCY PLUS BRACKET— 510(k) K933758

Name: FDA 510(k) clearance K933758
Creator: U.S. Food and Drug Administration
Published: 1994-01-18

Substantially Equivalent

Mid-American Dental Specialties, Inc.

FDA 510(k) clearance K933758 for REGENCY PLUS BRACKET, Substantially Equivalent on 1994-01-18. Applicant: Mid-American Dental Specialties, Inc.. Device class: 1.

Clearance details

Applicant: Mid-American Dental Specialties, Inc.
Product code: Code EJF
Device class: Class 1
Regulation: 21 CFR 872.5410
Advisory panel: Dental
Date received: 1993-08-03
Decision date: 1994-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hickory Hills, IL, US

Download summary PDF View on FDA.gov ↗

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