K-number	K960441
Device name	STERITEC INTEGRAPH MODEL CI-101
Applicant	Steritec Products Mfg Co, Inc.
Product code	JOJ
Device class	Class II
Decision date	May 8, 1997
Decision	Substantially Equivalent
Regulation	880.2800

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View the full FDA submission: accessdata.fda.gov

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STERITEC INTEGRAPH MODEL CI-101

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