K-number	K895507
Device name	LINK GIEBEL BLADE PLATE SYSTEM
Applicant	Link America, Inc.
Product code	KTT
Device class	Class II
Decision date	Mar 13, 1990
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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LINK GIEBEL BLADE PLATE SYSTEM

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