K-number	K833519
Device name	PULSE GENERATOR MODEL 688
Applicant	Burditt & Calkins-Siemens-Elema
Product code	DXY
Device class	Class III
Decision date	Jan 30, 1984
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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PULSE GENERATOR MODEL 688

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