K-number	K875147
Device name	TORQUE HEX WRENCH
Applicant	Cardiac Pacemakers, Inc.
Product code	DTF
Device class	Class I
Decision date	Jan 27, 1988
Decision	Substantially Equivalent
Regulation	870.3730

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View the full FDA submission: accessdata.fda.gov

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TORQUE HEX WRENCH

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