K-number	K790053
Device name	KELLEY-PLUS WITH MEASURETTE
Applicant	John N. Haswell, M.D.
Product code	KKX
Device class	Class II
Decision date	Jan 26, 1979
Decision	Substantially Equivalent
Regulation	878.4370

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View the full FDA submission: accessdata.fda.gov

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KELLEY-PLUS WITH MEASURETTE

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