NMI COAXIAL MICROINTRODUCER SET— 510(k) K123445

Name: FDA 510(k) clearance K123445
Creator: U.S. Food and Drug Administration
Published: 2013-04-01

Substantially Equivalent

Navilyst Medical, Inc.

FDA 510(k) clearance K123445 for NMI COAXIAL MICROINTRODUCER SET, Substantially Equivalent on 2013-04-01. Applicant: Navilyst Medical, Inc.. Device class: 2.

Clearance details

Applicant: Navilyst Medical, Inc.
Product code: Code DRE
Device class: Class 2
Regulation: 21 CFR 870.1310
Advisory panel: Cardiovascular
Date received: 2012-11-08
Decision date: 2013-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marlborough, MA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DRE

product code DRE

Death: 100
Injury: 832
Malfunction: 597
Other: 3
Total: 1,532

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.