K-number	K894738
Device name	MODEL 6888 LEAD TUNNELER
Applicant	Cardiac Pacemakers, Inc.
Product code	DWS
Device class	Class I
Decision date	Sep 13, 1989
Decision	Substantially Equivalent
Regulation	870.4500

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View the full FDA submission: accessdata.fda.gov

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MODEL 6888 LEAD TUNNELER

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