K-number	K946113
Device name	IMPLANT BODY RETRIEVER/REMOVER
Applicant	O Co., Inc.
Product code	DZE
Device class	Class II
Decision date	Mar 1, 1995
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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IMPLANT BODY RETRIEVER/REMOVER

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