PATIENT POSITIONING SYSTEM 1D OR 2D— 510(k) K800223

Name: FDA 510(k) clearance K800223
Creator: U.S. Food and Drug Administration
Published: 1980-03-03

Substantially Equivalent

Laboratoire National D'Essais

FDA 510(k) clearance K800223 for PATIENT POSITIONING SYSTEM 1D OR 2D, Substantially Equivalent on 1980-03-03. Applicant: Laboratoire National D'Essais. Device class: 1.

Clearance details

Applicant: Laboratoire National D'Essais
Product code: Code IWE
Device class: Class 1
Regulation: 21 CFR 892.5780
Advisory panel: Radiology
Date received: 1980-02-04
Decision date: 1980-03-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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