Class Class II

AIR Recon DL (K252379)

K252379 2025-12-23 Traditional
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Description

AIR Recon DL by Ge Medical Systems, LLC, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252379
Clearance Date2025-12-23
Clearance TypeTraditional
Product CodeLNH
Regulation Number892.1000

Categories

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