Class Class II

Stethophone Pro (K252595)

K252595 2025-09-12 Special
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Description

Stethophone Pro by Sparrow Acoustics, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252595
Clearance Date2025-09-12
Clearance TypeSpecial
Product CodeDQD
Regulation Number870.1875

Categories

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