7 months ago AMERICA NEWS NOW
|
An official website of the United States government
Here’s how you know
Featured
Products
- Food
- Drugs
- Medical Devices
- Radiation-Emitting Products
- Vaccines, Blood, and Biologics
- Animal and Veterinary
- Cosmetics
- Tobacco Products
Topics
- About FDA
- Combination Products
- Regulatory Information
- Safety
- Emergency Preparedness
- International Programs
- News and Events
- Training and Continuing Education
- Inspections and Compliance
- Science and Research
Information For
- Home
- Vaccines, Blood & Biologics
- Blood & Blood Products
- Approved Blood Products
- Substantially Equivalent 510(k) Device Information
- BK220752 - Erytra Eflexis
510(k) Number: BK220752
Applicant: Diagnostic Grifols, S.A.
Device Name: Erytra Eflexis
Decision Date: 11/1/2022
English (US) ·