510(k) K091268

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

K091268 is an FDA 510(k) premarket notification submitted by Hospira, Inc. for the device "HOSPIRA LATEX-FREE CRITICAL CARE AND ADVANCED SENSOR CATHETERS". The FDA issued a decision of Substantially Equivalent on September 18, 2009. The device falls under product code DQE (Catheter, Oximeter, Fiber-Optic), a Class II device regulated under 21 CFR 870.1230. Hospira, Inc. has at least 10 other 510(k) clearances on record.

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