LF MOTORIZED RADIOGRAPHIC FILM VIEWER— 510(k) K840607

Name: FDA 510(k) clearance K840607
Creator: U.S. Food and Drug Administration
Published: 1984-03-05

Substantially Equivalent

Sybron Corp.

FDA 510(k) clearance K840607 for LF MOTORIZED RADIOGRAPHIC FILM VIEWER, Substantially Equivalent on 1984-03-05. Applicant: Sybron Corp.. Device class: 1.

Clearance details

Applicant: Sybron Corp.
Product code: Code IXC
Device class: Class 1
Regulation: 21 CFR 892.1890
Advisory panel: Radiology
Date received: 1984-02-13
Decision date: 1984-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.