K-number	K982324
Device name	VECTRA PRO MODELS 2 AND 4
Applicant	Chattanooga Group, Inc.
Product code	GZJ
Device class	Class II
Decision date	Feb 1, 1999
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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VECTRA PRO MODELS 2 AND 4

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