Class Class II

Pression Wave PRO External Counter-Pulsation System (K250756)

K250756 2025-12-22 Traditional
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Description

Pression Wave PRO External Counter-Pulsation System by Pression, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250756
Clearance Date2025-12-22
Clearance TypeTraditional
Product CodeDRN
Regulation Number870.5225

Categories

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