K-number	K894622
Device name	VARICELLA ZOSTER VIRUS
Applicant	Bion Ent., Ltd.
Product code	GQW
Device class	Class II
Decision date	Oct 24, 1989
Decision	Substantially Equivalent
Regulation	866.3900

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View the full FDA submission: accessdata.fda.gov

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VARICELLA ZOSTER VIRUS

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