DEN210011
- 510(k) number
- DEN210011
- Device name
- Invitae Common Hereditary Cancers Panel
- Applicant
- Invitae Corporation CA · US
- Product code
- QVU — High Throughput Dna Sequencing For Hereditary Cancer
- Decision date
- 2023-09-29
- Date received
- 2021-03-29
- Decision
- Unknown
- Clearance type
- Direct
- Advisory committee
- Pathology
Official FDA record: DEN210011
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.