Class Class II

dS Base 1.5T; dS Base 3.0T; dS Head 1.5T; dS Head 3.0T; dS HeadNeck 1.5T; dS HeadNeck 3.0T (K254190)

K254190 2026-01-14 Special
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Description

dS Base 1.5T; dS Base 3.0T; dS Head 1.5T; dS Head 3.0T; dS HeadNeck 1.5T; dS HeadNeck 3.0T by Philips Medical Systems Nederland B.V., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK254190
Clearance Date2026-01-14
Clearance TypeSpecial
Product CodeMOS
Regulation Number892.1000

Categories

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