SIENET DICOM GATEWAY— 510(k) K952533

Substantially Equivalent

Siemens AG

FDA 510(k) clearance K952533 for SIENET DICOM GATEWAY, Substantially Equivalent on 1995-08-23. Applicant: Siemens AG. Device class: 1.

Clearance details

Applicant: Siemens AG
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1995-06-01
Decision date: 1995-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Iselin, NJ, 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.