K-number	K780766
Device name	(125 I) DIGITOXIN RIA KIT
Applicant	Diagnostic Products Corp.
Product code	LCW
Device class	Class II
Decision date	Jul 27, 1978
Decision	Substantially Equivalent
Regulation	862.3300

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View the full FDA submission: accessdata.fda.gov

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(125 I) DIGITOXIN RIA KIT

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