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510(k) Data Aggregation
K Number
K021934Device Name
MODIFICATION TO MEDSTATION
Manufacturer
Date Cleared
2002-08-12
(61 days)
Product Code
Regulation Number
892.2050Why did this record match?
Applicant Name (Manufacturer) :
AISOFTW@RE MEDICAL, S.P.A.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
For radiological image display, archival, retrieval and communications
Device Description
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