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OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH SEAL WITH HEPARIN

Page Type
Cleared 510(K)
510(k) Number
K062999
510(k) Type
Special
Applicant
Hospira, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/2006
Days to Decision
32 days
Submission Type
Summary

OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH SEAL WITH HEPARIN

Page Type
Cleared 510(K)
510(k) Number
K062999
510(k) Type
Special
Applicant
Hospira, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/2006
Days to Decision
32 days
Submission Type
Summary