K-number	K790562
Device name	PULSE GENERATOR MODEL 61 AND 128
Applicant	Ela Medical, Inc.
Product code	DXY
Device class	Class III
Decision date	May 8, 1979
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 61 AND 128

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