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FDA 510(k) Applications Submitted by KEN RAICHMAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070212
01/22/2007
CITOP10 GUIDEWIRE, 0.014(1.4MM TIP), CITOP6 GUIDEWIRE, 0.014(1.0MM TIP), CITOP SUPPORT ACCESSORY, 0.023(126CM)
OVALUM LTD.
K001120
04/07/2000
ENVOY PATIENT MONITOR
MENNEN MEDICAL LTD.
K021981
06/17/2002
IVENT 201 PORTABLE VENTILATOR
VERSAMED LTD.
K011957
06/22/2001
IVENT 201 PORTABLE VENTILATOR
VERSAMED LTD.
K982697
08/03/1998
MODIFICATION TO ENSEMBLE CENTRAL STATION MONITOR
MENNEN MEDICAL, INC.
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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