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25 devices found
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Manufacturer: Criticare Systems, Inc.
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Model 508 Patient Monitor
Criticare Systems, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K921309
Active
Cleared 17 Dec 1993
Active
510(k)
510(k)
II
506 Patient Monitor
Ciriticare Systems, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K051038
Active
Cleared 12 Aug 2005
Active
510(k)
510(k)
II
Sam(Tm) Model One
Sentel Tech. C/O Criticare Systems, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K880725
Active
Cleared 6 Sep 1988
Active
510(k)
510(k)
II
506 Non-Invasive Vital Signs Monitor
Criticare Systems, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K884216
Active
Cleared 16 Mar 1989
Active
510(k)
510(k)
II
8100 Vital Signs Monitor
Criticare Systems, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K001020
Active
Cleared 28 Apr 2000
Active
510(k)
510(k)
II
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