K-number	K964281
Device name	AESCULAP ANGLED NEUROENDOSCOPES
Applicant	Aesculap, Inc.
Product code	GWG
Device class	Class II
Decision date	Apr 21, 1997
Decision	Substantially Equivalent
Regulation	882.1480

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View the full FDA submission: accessdata.fda.gov

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AESCULAP ANGLED NEUROENDOSCOPES

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