K-number	K020090
Device name	MODIFICATION TO TRANSSEPTAL INTRODUCER SET
Applicant	Thomas Medical Products, Inc.
Product code	DYB
Device class	Class II
Decision date	Feb 11, 2002
Decision	Substantially Equivalent
Regulation	870.1340

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO TRANSSEPTAL INTRODUCER SET

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