K-number	K010785
Device name	KSEA DION-GRACIA SET
Applicant	KARL STORZ Endoscopy-America, Inc.
Product code	DXC
Device class	Class II
Decision date	Aug 21, 2001
Decision	Substantially Equivalent
Regulation	870.4450

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Source

View the full FDA submission: accessdata.fda.gov

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KSEA DION-GRACIA SET

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