WATERLASE MD TURBO PLUS MODEL 7200XXX (K101658) — FDA 510(k) Clearance | Predicase

K-number	K101658
Device name	WATERLASE MD TURBO PLUS MODEL 7200XXX
Applicant	Biolase Technology, Inc.
Product code	GEX
Device class	Class II
Decision date	Aug 11, 2010
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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