K-number	K791283
Device name	ANTI-HUMAN LAMBDA SERUM
Applicant	Diagnostica, Inc.
Product code	DEH
Device class	Class II
Decision date	Nov 27, 1979
Decision	Substantially Equivalent
Regulation	866.5550

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View the full FDA submission: accessdata.fda.gov

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ANTI-HUMAN LAMBDA SERUM

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