LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS— 510(k) K900809

Name: FDA 510(k) clearance K900809
Creator: U.S. Food and Drug Administration
Published: 1990-06-28

Substantially Equivalent

Lee Pharmaceuticals

FDA 510(k) clearance K900809 for LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS, Substantially Equivalent on 1990-06-28. Applicant: Lee Pharmaceuticals. Device class: 2.

Clearance details

Applicant: Lee Pharmaceuticals
Product code: Code DYW
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 1990-02-21
Decision date: 1990-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South El Monte, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.