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)

RBCFOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM

K-Number: K954332 · 1996-01-24

ApplicantBayer Corp.
Decision Date1996-01-24
Product CodeCGN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RBCFOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bayer Corp.. It received FDA 510(k) clearance on 1996-01-24 under 510(k) number K954332. The device is classified under product code CGN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RBCFOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM?

RBCFOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM is a medical device that received FDA 510(k) clearance on 1996-01-24. The listed applicant is Bayer Corp.. The 510(k) number is K954332.

When did RBCFOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM receive FDA 510(k) clearance?

RBCFOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM received FDA 510(k) clearance on 1996-01-24, under 510(k) number K954332.

Who is the listed applicant for RBCFOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM?

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

What is the FDA product code for RBCFOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM?

The FDA product code for RBCFOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM is CGN.

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 Bayer Corp. 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.

K024062ASCENSIA BREEZE BLOOD GLUCOSE METERK023944BAYER DIAGNOSTICS CLINITEST PREGNANCY TESTK024017BAYER ADVIA CENTAUR HER-2/NEU ASSAYK024234ASCENSIA GLUCOFACTS; ASCENSIA GLUCOFACTS PROFESSIONALK022288COMPLEXED PROSTATE SPECIFIC ANTIGEN (CPSA) ASSAY FOR THE BAYER ADVIA INTEGRATED MODULE SYSTEMK023584ASCENSIA DEX 2 DIABETES CARE SYSTEM

View all 96 devices →

Related Devices (Code: CGN)

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.

K233060Elecsys Folate IIIRoche DiagnosticsK223590Access Folate AssayBeckman Coulter, Inc.K192586LIAISON® FolateDiaSorin, Inc.K172201Atellica IM Folate AssaySiemens Healthcare Diagnostics, Inc.K161646Diazyme Folate Assay , Diazyme Folate Calibrator Set, Diazyme Folate Control SetDiazyme LaboratoriesK103716ROCHE ELECSYS FOLATE RBC; ROCHE ELECSYS FOLATE RBC CALSETRoche 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.

↑