K-number	K926410
Device name	ULTRATONE 8+ & 20
Applicant	Bowater Research, Inc.
Product code	IPF
Device class	Class II
Decision date	Aug 11, 1993
Decision	Substantially Equivalent
Regulation	890.5850

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View the full FDA submission: accessdata.fda.gov

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ULTRATONE 8+ & 20

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