SUN BED BY VERRE ET QUARTZ UVA-FRANCE— 510(k) K833229

Name: FDA 510(k) clearance K833229
Creator: U.S. Food and Drug Administration
Published: 1984-01-27

Substantially Equivalent

H & M Douglas Enterprises, Inc.

FDA 510(k) clearance K833229 for SUN BED BY VERRE ET QUARTZ UVA-FRANCE, Substantially Equivalent on 1984-01-27. Applicant: H & M Douglas Enterprises, Inc.. Device class: 1.

Clearance details

Applicant: H & M Douglas Enterprises, Inc.
Product code: Code FTZ
Device class: Class 1
Regulation: 21 CFR 886.4445
Advisory panel: Ophthalmic
Date received: 1983-08-24
Decision date: 1984-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FTZ

view all

K830468 — MODEL 2001983-04-12

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