K-number	K884261
Device name	PROWESS 2000
Applicant	Small Systems Group, Inc.
Product code	KPQ
Device class	Class II
Decision date	Aug 4, 1989
Decision	Substantially Equivalent
Regulation	892.5840

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View the full FDA submission: accessdata.fda.gov

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PROWESS 2000

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