FDA 510(k) Applications Submitted by GEOTEK Medikal Ltd sti

FDA 510(k) Number Submission Date Device Name Applicant
K170741 03/10/2017 GTK Disposable Needle Guides GEOTEK Medikal Ltd Sti
K223300 10/27/2022 Estacore-Pro Automatic Biopsy Needle, Geotek Semiautomatic Biopsy Needle, Maxicore-M Automatic Biopsy Gun Needle, Maxicore-M Automatic Biopsy Needle and Instrument GEOTEK Medikal Ltd sti


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