DICOM 3.0 SOFTWARE VERSION 2.0— 510(k) K973239

Name: FDA 510(k) clearance K973239
Creator: U.S. Food and Drug Administration
Published: 1997-11-26

Substantially Equivalent

Adac Laboratories

FDA 510(k) clearance K973239 for DICOM 3.0 SOFTWARE VERSION 2.0, Substantially Equivalent on 1997-11-26. Applicant: Adac Laboratories. Device class: 1.

Clearance details

Applicant: Adac Laboratories
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1997-08-28
Decision date: 1997-11-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milpitas, CA, US

Download summary PDF View on FDA.gov ↗

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