510(k) K061118

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

K061118 is an FDA 510(k) premarket notification submitted by Lifescan, Inc. for the device "ONETOUCH ULTRAMINI BLOOD GLUCOSE MONITORING SYSTEM". The FDA issued a decision of Substantially Equivalent on May 19, 2006. 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
May 19, 2006
Date Received
April 21, 2006
Clearance Type
Special
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