K-number	K991675
Device name	MODIFICATION OF: STERRAD BI TEST PACK
Applicant	Advanced Sterilization Products
Product code	FRC
Device class	Class II
Decision date	Jun 15, 1999
Decision	Substantially Equivalent
Regulation	880.2800

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION OF: STERRAD BI TEST PACK

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