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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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