Cleared Traditional

K090057 - ON-CALL PLUS BLOOD GLUCOSE MONITORING SYSTEM
(FDA 510(k) Clearance)

Apr 2009
Decision
90d
Days
Class 2
Risk

K090057 is an FDA 510(k) clearance for the ON-CALL PLUS BLOOD GLUCOSE MONITORING SYSTEM. This device is classified as a System, Test, Blood Glucose, Over The Counter (Class II - Special Controls, product code NBW).

Submitted by Acon Laboratories Co. (San Diego, US). The FDA issued a Cleared decision on April 8, 2009, 90 days after receiving the submission on January 8, 2009.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1345.

Submission Details

510(k) Number K090057 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 08, 2009
Decision Date April 08, 2009
Days to Decision 90 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

Product Code NBW — System, Test, Blood Glucose, Over The Counter
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1345

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