K-number	K991435
Device name	AII-PRO 100 PLUS AND ALL-PRO 200
Applicant	All-Pro Imaging Corp.
Product code	IXW
Device class	Class II
Decision date	May 20, 1999
Decision	Substantially Equivalent
Regulation	892.1900

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View the full FDA submission: accessdata.fda.gov

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AII-PRO 100 PLUS AND ALL-PRO 200

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