Class Class II

Fetal EchoScan (v1.2) (K252294)

K252294 2025-12-08 Traditional
Home/ Devices/ Fetal EchoScan (v1.2) (K252294)

Description

Fetal EchoScan (v1.2) by Brightheart, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252294
Clearance Date2025-12-08
Clearance TypeTraditional
Product CodePOK
Regulation Number892.2060

Categories

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