K-number	K010420
Device name	RUSCH MMG/O'NEIL CATHETER
Applicant	Rusch, Inc.
Product code	FCM
Device class	Class II
Decision date	May 9, 2001
Decision	Substantially Equivalent
Regulation	876.5130

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View the full FDA submission: accessdata.fda.gov

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RUSCH MMG/O'NEIL CATHETER

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