FDA 510(k) Applications Submitted by Creo Medical Ltd

FDA 510(k) Number Submission Date Device Name Applicant
K230328 02/06/2023 Speedboat Flush SB1 Instrument Creo Medical Ltd
K242061 07/15/2024 Reusable Interface Cable 1.5 m (PRD-IFC-002) Creo Medical Ltd
K242774 09/13/2024 SpydrBlade Flex Instrument (PRD-RG1-001) Creo Medical Ltd
K242983 09/26/2024 CROMA Electrosurgical Generator (PRD-EMR-050) Creo Medical Ltd
K171983 06/30/2017 Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory Creo Medical Ltd


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