K-number	K173495
Device name	Single Use Hot Biopsy Forceps FD-231
Applicant	Olympus Medical Systems Corp.
Product code	QEC
Device class	Class II
Decision date	Nov 30, 2018
Decision	Substantially Equivalent
Regulation	876.4300

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Source

View the full FDA submission: accessdata.fda.gov

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Single Use Hot Biopsy Forceps FD-231

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