Class Class II

FEops HEARTguideTM, FEops HEARTguideTM ALPACA (K223855)

K223855 2023-06-06 Traditional
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Description

FEops HEARTguideTM, FEops HEARTguideTM ALPACA by Feops NV — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223855
Clearance Date2023-06-06
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050

Categories

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