K-number	K780753
Device name	LAS-R HUMAN IGE TEST
Applicant	Hyland Therapeutic Div., Travenol Laboratories
Product code	DGC
Device class	Class II
Decision date	Jun 6, 1978
Decision	Substantially Equivalent
Regulation	866.5510

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View the full FDA submission: accessdata.fda.gov

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LAS-R HUMAN IGE TEST

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