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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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