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12 devices found
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Manufacturer: Oximetrix, Inc.
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Device · Manufacturer · Authorizations
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Registry
Class
Opticath Heparin Coated, Flow-Direct
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K823007
Active
Cleared 1 Nov 1982
Active
510(k)
510(k)
II
Catheter, Thermal Dilution Fiberoptic
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K781134
Active
Cleared 17 Aug 1978
Active
510(k)
510(k)
II
Hemo Static/Esu Scalpel System
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K842622
Active
Cleared 23 Oct 1984
Active
510(k)
510(k)
II
Opticath
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K820674
Active
Cleared 25 Mar 1982
Active
510(k)
510(k)
II
Oximetrix Shaw Hemostatic Surg. Sys.
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K791868
Active
Cleared 4 Jan 1980
Active
510(k)
510(k)
II
Model 3000 Opticath Computer
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K853018
Active
Cleared 13 Jan 1986
Active
510(k)
510(k)
II
Flow Directed Thermal-Dilution Infusion
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K821057
Active
Cleared 18 May 1982
Active
510(k)
510(k)
II
Oximetrix Accu Sat Cpb
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K811391
Active
Cleared 20 Jul 1981
Active
510(k)
510(k)
II
Oximeter, In Vivo Catheter
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K760234
Active
Cleared 23 Aug 1976
Active
510(k)
510(k)
II
Heater, Oximeter System
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K781879
Active
Cleared 8 Jan 1979
Active
510(k)
510(k)
II
Pump Infusion Wearable Infusion Pump
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K833966
Active
Cleared 25 Jan 1984
Active
510(k)
510(k)
I
Flow Directed Thermal-Dilution Catheter
Oximetrix, Inc.
·
,
United States
(FDA 510(k) applicant)
Not classified
FDA 510(k)
K821056
Active
Cleared 18 May 1982
Active
510(k)
510(k)
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