K-number	K201096
Device name	CO2mbiLED
Applicant	Karl Storz Endoscopy America, Inc.
Product code	FCX
Device class	Class II
Decision date	Jun 23, 2020
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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CO2mbiLED

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