K-number	K990231
Device name	WILTEK HOT BIOPSY FORCEPS
Applicant	Wiltek Medical, Inc.
Product code	KGE
Device class	Class II
Decision date	Apr 13, 1999
Decision	Substantially Equivalent
Regulation	876.4300

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View the full FDA submission: accessdata.fda.gov

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WILTEK HOT BIOPSY FORCEPS

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