K-number	K012639
Device name	SE-300 VACUUM THERAPY SYSTEM
Applicant	Vts, Inc.
Product code	LKY
Device class	Class II
Decision date	Nov 9, 2001
Decision	Substantially Equivalent
Regulation	876.5020

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View the full FDA submission: accessdata.fda.gov

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SE-300 VACUUM THERAPY SYSTEM

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