510(k) K091268

HOSPIRA LATEX-FREE CRITICAL CARE AND ADVANCED SENSOR CATHETERS by Hospira, Inc. — Product Code DQE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 18, 2009
Date Received
April 30, 2009
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Oximeter, Fiber-Optic
Device Class
Class II
Regulation Number
870.1230
Review Panel
CV
Submission Type