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)

FDI GLUCOSE CONTROL SOLUTION FOR AVIVA

K-Number: K110436 · 2011-04-20

ApplicantFujirebio Diagnostics,Inc.
Decision Date2011-04-20
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FDI GLUCOSE CONTROL SOLUTION FOR AVIVA is the device name listed in this FDA 510(k) record. The listed applicant is Fujirebio Diagnostics,Inc.. It received FDA 510(k) clearance on 2011-04-20 under 510(k) number K110436. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FDI GLUCOSE CONTROL SOLUTION FOR AVIVA?

FDI GLUCOSE CONTROL SOLUTION FOR AVIVA is a medical device that received FDA 510(k) clearance on 2011-04-20. The listed applicant is Fujirebio Diagnostics,Inc.. The 510(k) number is K110436.

When did FDI GLUCOSE CONTROL SOLUTION FOR AVIVA receive FDA 510(k) clearance?

FDI GLUCOSE CONTROL SOLUTION FOR AVIVA received FDA 510(k) clearance on 2011-04-20, under 510(k) number K110436.

Who is the listed applicant for FDI GLUCOSE CONTROL SOLUTION FOR AVIVA?

The FDA 510(k) record lists Fujirebio Diagnostics,Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FDI GLUCOSE CONTROL SOLUTION FOR AVIVA?

The FDA product code for FDI GLUCOSE CONTROL SOLUTION FOR AVIVA is JJX.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Fujirebio Diagnostics,Inc. 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.

K250925ADVIA Centaur Cytokeratin Fragment 21-1K242706Lumipulse G pTau217/ß-Amyloid 1-42 Plasma RatioK192524Lumipulse G CA15-3K192380ST AIA-PACK BNPK200997Lumipulse G CA19-9-NK190702Lumipulse G whole PTH

View all 40 devices →

Related Devices (Code: JJX)

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.

K170678Beta-CrossLaps CalCheck 5Roche DiagnosticsK162173Elecsys CYFRA 21-1 CalCheck 5Roche DiagnosticsK162514Multichem A1cTechnopath ManufacturingK161874Audit MicroControls Linearity DROP LQ Blood GlucoseAalto Scientific, Ltd.K161526LIAISON CMV IgM Serum Control SetDiaSorin, Inc.K161522LIAISON EBV IgM Serum Control SetDiaSorin, Inc.

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.

↑