Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Alegria Flash SSA-60; Alegria Flash SSA-52; Alegria FLash SSB

K-Number: K250814 · 2026-05-08

ApplicantZeus Scientific
Decision Date2026-05-08
Product CodeOBE
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

Alegria Flash SSA-60; Alegria Flash SSA-52; Alegria FLash SSB is the device name listed in this FDA 510(k) record. The listed applicant is Zeus Scientific. It received FDA 510(k) clearance on 2026-05-08 under 510(k) number K250814. The device is classified under product code OBE. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Alegria Flash SSA-60; Alegria Flash SSA-52; Alegria FLash SSB?

Alegria Flash SSA-60; Alegria Flash SSA-52; Alegria FLash SSB is a medical device that received FDA 510(k) clearance on 2026-05-08. The listed applicant is Zeus Scientific. The 510(k) number is K250814.

When did Alegria Flash SSA-60; Alegria Flash SSA-52; Alegria FLash SSB receive FDA 510(k) clearance?

Alegria Flash SSA-60; Alegria Flash SSA-52; Alegria FLash SSB received FDA 510(k) clearance on 2026-05-08, under 510(k) number K250814.

Who is the listed applicant for Alegria Flash SSA-60; Alegria Flash SSA-52; Alegria FLash SSB?

The FDA 510(k) record lists Zeus Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Alegria Flash SSA-60; Alegria Flash SSA-52; Alegria FLash SSB?

The FDA product code for Alegria Flash SSA-60; Alegria Flash SSA-52; Alegria FLash SSB is OBE.

Other records listing Zeus Scientific 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.

K250666Alegria Flash CTD ScreenK250408Alegria Flash ENA ScreenK243776Anti-Neutrophil Cytoplasmic Antibodies (Ethanol-Fixed); Anti-Neutrophil Cytoplasmic Antibodies (Formalin-Fixed)K231616ZEUS IFA(TM) nDNA Test System, ZEUS dIFineK230863ZEUS Solinas Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS Solinas Borrelia VlsE1/pepC10 IgG/IgM Control KitK201956Zeus IFA ANA HEp-2 Test System, Zeus dIFine

View all 12 devices →

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.

↑