Class Class II

Swoop® Portable MR Imaging System™ (K230208)

K230208 2023-02-22 Special
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Description

Swoop® Portable MR Imaging System™ by Hyperfine, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230208
Clearance Date2023-02-22
Clearance TypeSpecial
Product CodeLNH
Regulation Number892.1000

Categories

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