K-number	K953908
Device name	DAVIS & GECK LIGATING CLIP REMOVER
Applicant	Davis & Geck, Inc.
Product code	FZP
Device class	Class II
Decision date	Nov 30, 1995
Decision	Substantially Equivalent
Regulation	878.4300

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View the full FDA submission: accessdata.fda.gov

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DAVIS & GECK LIGATING CLIP REMOVER

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