K-number	K191948
Device name	GlideScope BFlex 5.8 Single-Use Bronchoscope
Applicant	Verathon Medical (Canada) Ulc
Product code	EOQ
Device class	Class II
Decision date	Aug 21, 2019
Decision	Substantially Equivalent
Regulation	874.4680

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Source

View the full FDA submission: accessdata.fda.gov

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GlideScope BFlex 5.8 Single-Use Bronchoscope

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