K220265
- 510(k) number
- K220265
- Device name
- ADVIA Centaur® NT-proBNPII (PBNPII)
- Applicant
- Siemens Healthcare Diagnostics, Inc. NY · US
- Product code
- NBC — Test, Natriuretic Peptide
- Decision date
- 2023-09-24
- Date received
- 2022-01-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Clinical Chemistry
510(k) Summary (official FDA PDF): K220265.pdf
Official FDA record: K220265
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.