DIGITAL IMAGING SYSTEM INTERFACE— 510(k) K953080

Name: FDA 510(k) clearance K953080
Creator: U.S. Food and Drug Administration
Published: 1995-09-28

Substantially Equivalent

Camtronics, Ltd.

FDA 510(k) clearance K953080 for DIGITAL IMAGING SYSTEM INTERFACE, Substantially Equivalent on 1995-09-28. Applicant: Camtronics, Ltd.. Device class: 1.

Clearance details

Applicant: Camtronics, Ltd.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1995-07-03
Decision date: 1995-09-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hartland, WI, US

Download summary PDF View on FDA.gov ↗

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