Class Class II

SleepRes PAP System (K251770)

K251770 2025-12-15 Traditional
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Description

SleepRes PAP System by Sleepres, Inc., an FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251770
Clearance Date2025-12-15
Clearance TypeTraditional
Product CodeBZD
Regulation Number868.5905

Categories

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