FDA 510(k) Applications Submitted by SurgVision GmbH

FDA 510(k) Number Submission Date Device Name Applicant
K222240 07/26/2022 EXPLORER AIR« II SurgVision GmbH
K234090 12/22/2023 EXPLORER AIR« II (8001, 8002, 8003); EXPLORER AIR« Sterile Drape (8004) SurgVision GmbH
K214097 12/28/2021 Explorer Air II SurgVision GmbH


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