FDA 510(k) Applications Submitted by PENTRON LABORATORY TECHNOLOGIES

FDA 510(k) Number Submission Date Device Name Applicant
K020555 02/20/2002 SONATA MICRO HYBRID COMPOSITE PENTRON LABORATORY TECHNOLOGIES
K023499 10/18/2002 GOLD CORE PLUS PENTRON LABORATORY TECHNOLOGIES
K023742 11/07/2002 SCULPTURE PLUS NANO-HYBRID COMPOSITE PENTRON LABORATORY TECHNOLOGIES
K023501 10/18/2002 GOLD CORE 35 PENTRON LABORATORY TECHNOLOGIES
K023502 10/18/2002 JEWEL CAST PLUS PENTRON LABORATORY TECHNOLOGIES


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