PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT— 510(k) K912256

Name: FDA 510(k) clearance K912256
Creator: U.S. Food and Drug Administration
Published: 1991-07-24

Substantially Equivalent

Lee Pharmaceuticals

FDA 510(k) clearance K912256 for PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT, Substantially Equivalent on 1991-07-24. Applicant: Lee Pharmaceuticals. Device class: 2.

Clearance details

Applicant: Lee Pharmaceuticals
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 1991-05-22
Decision date: 1991-07-24
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.