FDA 510(k) Applications Submitted by RODNEY GUYTON

FDA 510(k) Number Submission Date Device Name Applicant
K002298 07/28/2000 SUPER 1 DENTAL ALLOY PRODUCTS, INC.
K002299 07/28/2000 SUPER 3 DENTAL ALLOY PRODUCTS, INC.
K002300 07/28/2000 SUPER 6 DENTAL ALLOY PRODUCTS, INC.
K002301 07/28/2000 SUPER 12 DENTAL ALLOY PRODUCTS, INC.
K002302 07/28/2000 SUPER 14 DENTAL ALLOY PRODUCTS, INC.


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