K-number	K863570
Device name	LE VEEN WOUND SPLINT
Applicant	Tek-Aid, Inc.
Product code	KGS
Device class	Class I
Decision date	Sep 29, 1986
Decision	Substantially Equivalent
Regulation	878.4930

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View the full FDA submission: accessdata.fda.gov

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LE VEEN WOUND SPLINT

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