K-number	K915852
Device name	ACCUPACE GROUP A STREPTOCOCCUS ID TEST
Applicant	Gen-Probe, Inc.
Product code	MDK
Device class	Class I
Decision date	Apr 2, 1992
Decision	Substantially Equivalent
Regulation	866.3740

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View the full FDA submission: accessdata.fda.gov

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ACCUPACE GROUP A STREPTOCOCCUS ID TEST

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