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)

TRUQUANT BR RIA

K-Number: K965141 · 1997-10-31

ApplicantBiomira USA, Inc.
Decision Date1997-10-31
Product CodeMOI
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TRUQUANT BR RIA is the device name listed in this FDA 510(k) record. The listed applicant is Biomira USA, Inc.. It received FDA 510(k) clearance on 1997-10-31 under 510(k) number K965141. The device is classified under product code MOI. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRUQUANT BR RIA?

TRUQUANT BR RIA is a medical device that received FDA 510(k) clearance on 1997-10-31. The listed applicant is Biomira USA, Inc.. The 510(k) number is K965141.

When did TRUQUANT BR RIA receive FDA 510(k) clearance?

TRUQUANT BR RIA received FDA 510(k) clearance on 1997-10-31, under 510(k) number K965141.

Who is the listed applicant for TRUQUANT BR RIA?

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

What is the FDA product code for TRUQUANT BR RIA?

The FDA product code for TRUQUANT BR RIA is MOI.

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

Related Devices (Code: MOI)

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.

K240403Access BR MonitorBeckman Coulter, Inc.K233946IMMULITE® 2000 BR-MASiemens Healthcare Diagnostics Products, Ltd.K192524Lumipulse G CA15-3Fujirebio Diagnostics,Inc.K193489ADVIA Centaur BRSiemens Healthcare Diagnostics, Inc.K192777ADVIA Centaur CA 15-3 assaySiemens Healthcare Diagnostics, Inc.K181492Elecsys CA 15-3 IIRoche Diagnostics

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.

↑