K-number	K862641
Device name	U.S. DIAGNOSTIC INC. HEMOGLOBIN TEST (DRY PACK)
Applicant	U. S. Diagnostics, Inc.
Product code	KHG
Device class	Class II
Decision date	Aug 21, 1986
Decision	Substantially Equivalent
Regulation	864.7500

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View the full FDA submission: accessdata.fda.gov

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U.S. DIAGNOSTIC INC. HEMOGLOBIN TEST (DRY PACK)

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