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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K183256

GlideScope BFlex Single-Use Bronchoscope System · Verathon Medical (Canada) Ulc · decided 2019-01-04 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
BFlex™BFlex™ 2 Regular 5.0Verathon Medical (Canada) ULCEOQ00879123008565
GlideScope® BFlex™ 5.0Verathon Medical (Canada) ULCEOQ00879123006332