FDA 510(k) Applications Submitted by Cipher Surgical Limited

FDA 510(k) Number Submission Date Device Name Applicant
K221824 06/23/2022 OpClear Platform (CU3 DI3), OpClear Control Unit with Footswitch (CS-CU33), OpClear Disposable Procedure Kits (CS-10-00-300, CS-10-30-300, CS-10-00-315, CS-10-30-315, CS-10-00-330, CS-10-30-330, CS-05-00-290, CS-05-30-290), Contd from 3 above: CS-05-00-30 Cipher Surgical Limited


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