FDA 510(k) Applications Submitted by Creo Medical Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K192905 10/15/2019 Creo Electrosurgical System with HS1 Hemostasis Accessory Creo Medical Ltd.
K200298 02/06/2020 ABI Instrument, Creo Electrosurgical System Creo Medical Ltd.
K200003 01/02/2020 NP1 Instrument, Creo Electrosurgical System Creo Medical Ltd.
K221672 06/09/2022 Creo Electrosurgical System with NP1 Instrument Creo Medical Ltd.
K223138 10/04/2022 AB1 Electrosurgical Instrument, Creo Electrosurgical System Creo Medical Ltd.


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