K-number	K990732
Device name	LAP-WAVE 3000 (P07)
Applicant	W.O.M. World of Medicine GmbH
Product code	HET
Device class	Class II
Decision date	Jul 23, 1999
Decision	Substantially Equivalent
Regulation	884.1720

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View the full FDA submission: accessdata.fda.gov

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LAP-WAVE 3000 (P07)

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