FDA 510(k) Applications Submitted by KENNETH RAICHMAN

FDA 510(k) Number Submission Date Device Name Applicant
K000563 02/22/2000 MODIFICATION TO ENVOY PATIENT MONITOR MENNEN MEDICAL LTD.
K991775 05/25/1999 MODIFICATION TO COMPUTERIZED CATHETERIZATION LABORATORY - HORIZON 9000 WS MENNEN MEDICAL, INC.
K983864 11/02/1998 ETCO2 VITAL SIGNS MODULE MENNEN MEDICAL, INC.
K974510 12/01/1997 ENVOY PATIENT MONITOR MENNEN MEDICAL, INC.


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