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51 devices found
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Manufacturer: Critikon Company, LLC
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Class
Intravenous Catheters Modifications
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K921295
Active
Cleared 17 May 1993
Active
510(k)
510(k)
II
The Simplicity Pump #2100 Infusion Pump
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K801546
Active
Cleared 27 Aug 1980
Active
510(k)
510(k)
II
Dinamap Plus Physiological Monitor Model 8700
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K912188
Active
Cleared 4 Dec 1991
Active
510(k)
510(k)
II
Changes To Protectiv(Tm) & Jelco(Tm) Winged Cath
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K933050
Active
Cleared 14 Dec 1993
Active
510(k)
510(k)
II
Critikon Dual Channel Recorder
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K792105
Active
Cleared 26 Oct 1979
Active
510(k)
510(k)
I
Dinamap Vital Signs Monitor #1846P
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K832656
Active
Cleared 7 Nov 1983
Active
510(k)
510(k)
II
Rate-Mate Nitroglycerin I.V. Administration Set
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K873729
Active
Cleared 29 Dec 1987
Active
510(k)
510(k)
II
Critikon Cardiac Output Computer W/Hemodynamic
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K844116
Active
Cleared 28 May 1985
Active
510(k)
510(k)
II
Dinamap Advanced Nibp Module
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K000500
Active
Cleared 26 May 2000
Active
510(k)
510(k)
II
Monitor, Oxychek Oxygen
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K782114
Active
Cleared 18 Jan 1979
Active
510(k)
510(k)
II
I.V. Catheter Placement Unit Polyureth
Critikon Company, LLC
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K830972
Active
Cleared 27 Apr 1983
Active
510(k)
510(k)
II
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