MEDSTATION— 510(k) K973090

Substantially Equivalent

Program S.R.L.

FDA 510(k) clearance K973090 for MEDSTATION, Substantially Equivalent on 1997-10-28. Applicant: Program S.R.L.. Device class: 1.

Clearance details

Applicant: Program S.R.L.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1997-08-18
Decision date: 1997-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Teaneck, 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.