FDA 510(k) Applications for Medical Device Product Code "FBM"
(Cannula And Trocar, Suprapubic, Non-Disposable)

FDA 510(k) Number Applicant Device Name Decision Date
K960400 SNOWDEN-PENCER DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS) 03/12/1996


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