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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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