K-number	K842220
Device name	MULTILITH 2 PULSE GENERATOR 1141 & 2141
Applicant	Ela Medical, Inc.
Product code	DXY
Device class	Class III
Decision date	Nov 29, 1984
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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MULTILITH 2 PULSE GENERATOR 1141 & 2141

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