PRECISION XCEED PRO BLOOD GLUCOSE AND B-KETONE MONITORING SYSTEM WITH MODELS BGMS:70900-03, 70090-02, G3CH STRIPS— 510(k) K080960

Substantially Equivalent

Abbott Diabetes Care, Inc.

FDA 510(k) clearance K080960 for PRECISION XCEED PRO BLOOD GLUCOSE AND B-KETONE MONITORING SYSTEM WITH MODELS BGMS:70900-03, 70090-02, G3CH STRIPS, Substantially Equivalent on 2008-09-05. Applicant: Abbott Diabetes Care, Inc.. Device class: 2.

Clearance details

Applicant
Abbott Diabetes Care, Inc.
Product code
Code NBW
Device class
Class 2
Regulation
21 CFR 862.1345
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Alameda, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code NBW

product code NBW
Death
18
Injury
4,740
Malfunction
42,679
Other
6
Total
47,443

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.