K-number	K780430
Device name	LITHICRON F PROGRAMMABLE PULSE GEN
Applicant	Medcor, Inc.
Product code	DXY
Device class	Class III
Decision date	Dec 22, 1978
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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LITHICRON F PROGRAMMABLE PULSE GEN

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