Class Class II

SpectraWAVE Imaging System (K221257)

K221257 2023-02-28 Traditional
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Description

SpectraWAVE Imaging System by Spectrawave, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221257
Clearance Date2023-02-28
Clearance TypeTraditional
Product CodeNQQ
Regulation Number892.1560

Categories

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