K-number	K930501
Device name	DU PONT ACA NEV/EEV VERIFIER
Applicant	Dupont Medical Products
Product code	JIS
Device class	Class II
Decision date	Aug 9, 1993
Decision	Substantially Equivalent
Regulation	862.1150

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View the full FDA submission: accessdata.fda.gov

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DU PONT ACA NEV/EEV VERIFIER

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