K-number	K952008
Device name	KARL STORZ DRILL
Applicant	KARL STORZ Endoscopy-America, Inc.
Product code	GEY
Device class	Class I
Decision date	Jul 26, 1995
Decision	Substantially Equivalent
Regulation	878.4820

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View the full FDA submission: accessdata.fda.gov

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KARL STORZ DRILL

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