Invitae Common Hereditary Cancers Panel— 510(k) DEN210011
UnknownInvitae Corporation
FDA 510(k) clearance DEN210011 for Invitae Common Hereditary Cancers Panel, Unknown on 2023-09-29. Applicant: Invitae Corporation. Device class: 2.
Clearance details
- Applicant
- Invitae Corporation
- Product code
- Code QVU
- Device class
- Class 2
- Regulation
- 21 CFR 866.6095
- Advisory panel
- Pathology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- San Francisco, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.