K-number	K172084
Device name	Delta III Lithotripter
Applicant	Dornier Medtech America, Inc.
Product code	LNS
Device class	Class II
Decision date	Aug 8, 2017
Decision	Substantially Equivalent
Regulation	876.5990

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Source

View the full FDA submission: accessdata.fda.gov

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Delta III Lithotripter

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