Class Class II

Symbia Pro.specta VA20A Family (K231102)

K231102 2023-05-17 Special
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Description

Symbia Pro.specta VA20A Family by Siemens Medical Solutions USA, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK231102
Clearance Date2023-05-17
Clearance TypeSpecial
Product CodeKPS
Regulation Number892.1200

Categories

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