Class Class II

Sleep Watch (K251574)

K251574 2025-07-31 Special
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Description

Sleep Watch by Ambulatory Monitoring, Inc., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251574
Clearance Date2025-07-31
Clearance TypeSpecial
Product CodeLEL
Regulation Number882.5050

Categories

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