K-number	K921934
Device name	INTRADUCER
Applicant	Taut, Inc.
Product code	GBX
Device class	Class I
Decision date	Jul 15, 1992
Decision	Substantially Equivalent
Regulation	878.4200

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Source

View the full FDA submission: accessdata.fda.gov

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INTRADUCER

Everything you need for a 510(k) submission. Nothing you don't.