K-number	K854195
Device name	PROGRAMALITH III MODELS 238 & 239
Applicant	Pacesetter Systems
Product code	DXY
Device class	Class III
Decision date	Jan 7, 1986
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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PROGRAMALITH III MODELS 238 & 239

Everything you need for a 510(k) submission. Nothing you don't.