K-number	K182696
Device name	Telepack X LED
Applicant	KARL STORZ Endoscopy-America, Inc.
Product code	FET
Device class	Class II
Decision date	Nov 20, 2018
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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Telepack X LED

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