Class Class II

The BAG manual resuscitator and accessories (K251631)

K251631 2025-11-24 Traditional
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Description

The BAG manual resuscitator and accessories by Laerdal Medical AS, an FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251631
Clearance Date2025-11-24
Clearance TypeTraditional
Product CodeBTM
Regulation Number868.5915

Categories

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