K-number	K841832
Device name	GLOTTAL FREQUENCY ANALYSER
Applicant	Teltec Electronic Equipment AB
Product code	KLX
Device class	Class II
Decision date	Jul 18, 1984
Decision	Substantially Equivalent
Regulation	874.1325

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View the full FDA submission: accessdata.fda.gov

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GLOTTAL FREQUENCY ANALYSER

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