K-number	K914896
Device name	FRIEDMANN ANALYSER 3
Applicant	Clement Clarke, Inc.
Product code	HOK
Device class	Class I
Decision date	Jan 23, 1992
Decision	Substantially Equivalent
Regulation	886.1810

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View the full FDA submission: accessdata.fda.gov

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FRIEDMANN ANALYSER 3

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