510(k) K073231

ONETOUCH ULTRALINK BLOOD GLUCOSE MONITORING SYSTEM by Lifescan, Inc. — Product Code NBW

K073231 is an FDA 510(k) premarket notification submitted by Lifescan, Inc. for the device "ONETOUCH ULTRALINK BLOOD GLUCOSE MONITORING SYSTEM". The FDA issued a decision of Substantially Equivalent on April 18, 2008. The device falls under product code NBW (System, Test, Blood Glucose, Over The Counter), a Class II device regulated under 21 CFR 862.1345. Lifescan, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 18, 2008
Date Received
November 15, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Blood Glucose, Over The Counter
Device Class
Class II
Regulation Number
862.1345
Review Panel
CH
Submission Type