K-number	K963158
Device name	ABBOTT AXSYM DIGITOXIN (MODIFY)
Applicant	Abbott Laboratories
Product code	LFM
Device class	Class II
Decision date	Sep 10, 1996
Decision	Substantially Equivalent
Regulation	862.3300

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View the full FDA submission: accessdata.fda.gov

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ABBOTT AXSYM DIGITOXIN (MODIFY)

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