Perineologic Access Needle— 510(k) K160423
Substantially EquivalentCorbin Clinical Resources, LLC
FDA 510(k) clearance K160423 for Perineologic Access Needle, Substantially Equivalent on 2016-09-02. Applicant: Corbin Clinical Resources, LLC.
Clearance details
- Applicant
- Corbin Clinical Resources, LLC
- Product code
- Code FCG
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cumberland, MD, US
Adverse events under product code FCG
product code FCG- Death
- 13
- Injury
- 576
- Malfunction
- 1,966
- Total
- 2,555
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.