K-number	K062159
Device name	RB12 SUCTION RECTAL BIOPSY SYSTEM
Applicant	Aus Systems Pty , Ltd.
Product code	FCK
Device class	Class II
Decision date	Sep 5, 2006
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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RB12 SUCTION RECTAL BIOPSY SYSTEM

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