LEE-FILL ULTRAVIOLET-CURED REST. MAT.— 510(k) K760417

Name: FDA 510(k) clearance K760417
Creator: U.S. Food and Drug Administration
Published: 1976-08-23

Substantially Equivalent

Lee Pharmaceuticals

FDA 510(k) clearance K760417 for LEE-FILL ULTRAVIOLET-CURED REST. MAT., Substantially Equivalent on 1976-08-23. Applicant: Lee Pharmaceuticals. Device class: 2.

Clearance details

Applicant: Lee Pharmaceuticals
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 1976-08-09
Decision date: 1976-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K261246 — SRGC-062026-06-18

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K894315 — RESTOBOND 3/DENTIN-ENAMEL BONDING AGENT1989-10-31
K881903 — PROSTHODENT VL1988-07-01

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