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)

ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST

K-Number: K924036 · 1992-12-01

ApplicantJ.S. Medical Assoc.
Decision Date1992-12-01
Product CodeDHR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST is the device name listed in this FDA 510(k) record. The listed applicant is J.S. Medical Assoc.. It received FDA 510(k) clearance on 1992-12-01 under 510(k) number K924036. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST?

ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST is a medical device that received FDA 510(k) clearance on 1992-12-01. The listed applicant is J.S. Medical Assoc.. The 510(k) number is K924036.

When did ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST receive FDA 510(k) clearance?

ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST received FDA 510(k) clearance on 1992-12-01, under 510(k) number K924036.

Who is the listed applicant for ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST?

The FDA 510(k) record lists J.S. Medical Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST?

The FDA product code for ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST is DHR.

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 J.S. Medical Assoc. 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.

K932752VISI-SPOTK932688EYE SPOT IM TESTK932180EYE SPOT CRP TESTK932551ACCUTEX IM LATEX TESTK926112ACCUTEX BETA-HCG TESTK924332ACCUTEX CRP LATEX TEST

View all 18 devices →

Related Devices (Code: DHR)

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.

K192727K-ASSAY (R) RF (Ver.2), K-ASSAY (R) RF Calibrator (Ver.2)Kamiya Biomedical CompanyK190088QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA ReagentsInova Diagnostics, Inc.K182747EliA RF IgM ImmunoassayPhadia ABK162263Optilite Rheumatoid Factor KitThe Binding Site Group , Ltd.K160070Rheumatoid Factor (RF) Kit for use on SPAPLUSThe Binding Site Group , Ltd.K102673RHEUMATOID FACTOR IMMUNOLOGICAL TEST SYSTEMPhadia US, 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.

↑