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510(k) Data Aggregation

K Number

Device Name

MAGNETOM RHAPSODY SYSTEM

Manufacturer

SIEMENS MEDICAL SOLUTIONS USA, INC.

Date Cleared

2001-01-23

(60 days)

Product Code

Regulation Number

Type

Panel

Reference & Predicate Devices

N/A

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AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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