K-number	K861098
Device name	SEROIDEN STREPTO KIT 'EIKEN'
Applicant	Syn-Kit, Inc.
Product code	GTZ
Device class	Class I
Decision date	Aug 12, 1986
Decision	Substantially Equivalent
Regulation	866.3740

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Source

View the full FDA submission: accessdata.fda.gov

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SEROIDEN STREPTO KIT 'EIKEN'

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