K-number	K790833
Device name	VISIO-BOND
Applicant	Espe GmbH (Us)
Product code	KLE
Device class	Class II
Decision date	Apr 30, 1979
Decision	Substantially Equivalent — with Special Conditions
Regulation	872.3200

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View the full FDA submission: accessdata.fda.gov

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VISIO-BOND

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