FDA 510(k) Applications Submitted by B. K. MA

FDA 510(k) Number Submission Date Device Name Applicant
K000351 02/04/2000 HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE HANWELLA RUBBER PRODUCTS LTD.
K962725 07/15/1996 SOMA SOMA INTERNATIONAL LTD.
K992868 08/26/1999 DENTAPURE DP40 CARTRIDGE MRLB INTL., INC.
K992893 08/27/1999 DENTAPURE DP 90 CARTRIDGE, DENTAPURE DP 365 CARTRIDGE MRLB INTL., INC.


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