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OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH FLUIDIC SEAL WITH/WITHOUT HEPARIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061159
510(k) Type
Traditional
Applicant
HOSPIRA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2006
Days to Decision
61 days
Submission Type
Summary

OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH FLUIDIC SEAL WITH/WITHOUT HEPARIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061159
510(k) Type
Traditional
Applicant
HOSPIRA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2006
Days to Decision
61 days
Submission Type
Summary