NORTON MANIFOLD— 510(k) K820864
Substantially EquivalentNorton Performance Plastics Corp.
FDA 510(k) clearance K820864 for NORTON MANIFOLD, Substantially Equivalent on 1982-04-15. Applicant: Norton Performance Plastics Corp..
Clearance details
- Applicant
- Norton Performance Plastics Corp.
- Product code
- Code DTL
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Adverse events under product code DTL
product code DTL- Malfunction
- 770
- Total
- 770
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.