K-number	K895725
Device name	BIOPSY NEEDLE GUIDE FOR ADMS ULTRASOUND PROBES
Applicant	Interson Corp.
Product code	FCG
Device class	Class II
Decision date	Nov 6, 1989
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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BIOPSY NEEDLE GUIDE FOR ADMS ULTRASOUND PROBES

Everything you need for a 510(k) submission. Nothing you don't.