K-number	K970596
Device name	DHD EMERALD PRODUCT
Applicant	Dhd Diemolding Healthcare Div.
Product code	BWF
Device class	Class II
Decision date	May 16, 1997
Decision	Substantially Equivalent
Regulation	868.5690

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View the full FDA submission: accessdata.fda.gov

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DHD EMERALD PRODUCT

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