Nova Allegro UACR Assay, Nova Allegro Analyzer
K-Number: K221813 · 2024-11-19
Device Summary
Frequently Asked Questions
What is the Nova Allegro UACR Assay, Nova Allegro Analyzer?
Nova Allegro UACR Assay, Nova Allegro Analyzer is a medical device that received FDA 510(k) clearance on 2024-11-19. The listed applicant is Nova Biomedical Corporation. The 510(k) number is K221813.
When did Nova Allegro UACR Assay, Nova Allegro Analyzer receive FDA 510(k) clearance?
Nova Allegro UACR Assay, Nova Allegro Analyzer received FDA 510(k) clearance on 2024-11-19, under 510(k) number K221813.
Who is the listed applicant for Nova Allegro UACR Assay, Nova Allegro Analyzer?
The FDA 510(k) record lists Nova Biomedical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nova Allegro UACR Assay, Nova Allegro Analyzer?
The FDA product code for Nova Allegro UACR Assay, Nova Allegro Analyzer is CGX.
Other records listing Nova Biomedical Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CGX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.