Class Class II

OptoMonitor 3 (K251367)

K251367 2026-01-16 Traditional
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Description

OptoMonitor 3 by Opsens, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251367
Clearance Date2026-01-16
Clearance TypeTraditional
Product CodeDXO
Regulation Number870.2870

Categories

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