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Found 1 results

510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

dS Base 1.5T; dS Base 3.0T; dS Head 1.5T; dS Head 3.0T; dS HeadNeck 1.5T; dS HeadNeck 3.0T

Manufacturer

Philips Medical Systems Nederland B.V.

Date Cleared

2026-01-14

(22 days)

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Panel

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N/A

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AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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