K-number	K801799
Device name	ATRIAL/VENTRICULAR SEQENTIAL #080-20000
Applicant	Medical Testing System, Inc.
Product code	LDF
Device class	Class II
Decision date	Jan 2, 1981
Decision	Substantially Equivalent
Regulation	870.3680

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View the full FDA submission: accessdata.fda.gov

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ATRIAL/VENTRICULAR SEQENTIAL #080-20000

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