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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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