TRUE METRIX SELF-MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE SYSTEM— 510(k) K140100

Substantially Equivalent

Nipro Diagnostics, Inc.

FDA 510(k) clearance K140100 for TRUE METRIX SELF-MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE SYSTEM, Substantially Equivalent on 2014-08-01. Applicant: Nipro Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant
Nipro Diagnostics, 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
Fort Lauderdale, FL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code NBW

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More clearances from Nipro Diagnostics, Inc.

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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 →

Recalls naming K140100

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K140100.

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