CONCENTRIC HYDROPHILIC GUIDEWIRE, MODELS 90011, 90012— 510(k) K003084

Substantially Equivalent

Concentric Medical, Inc.

FDA 510(k) clearance K003084 for CONCENTRIC HYDROPHILIC GUIDEWIRE, MODELS 90011, 90012, Substantially Equivalent on 2001-05-16. Applicant: Concentric Medical, Inc..

Clearance details

Applicant: Concentric Medical, Inc.
Product code: Code DQX
Advisory panel: Cardiovascular
Date received: 2000-10-03
Decision date: 2001-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Moutian View, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQX

product code DQX

Death: 298
Injury: 4,385
Malfunction: 7,203
Other: 5
Total: 11,891

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.