K-number	K930070
Device name	HEMOCARD HEMOGLOBIN E
Applicant	Isolab, Inc.
Product code	CKA
Device class	Class I
Decision date	Apr 8, 1993
Decision	Substantially Equivalent
Regulation	862.1030

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View the full FDA submission: accessdata.fda.gov

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HEMOCARD HEMOGLOBIN E

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