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)

DIAPHARMA FACTOR X KIT

K-Number: K040362 · 2004-07-12

ApplicantDiapharma Group, Inc.
Decision Date2004-07-12
Product CodeGJT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

DIAPHARMA FACTOR X KIT is the device name listed in this FDA 510(k) record. The listed applicant is Diapharma Group, Inc.. It received FDA 510(k) clearance on 2004-07-12 under 510(k) number K040362. The device is classified under product code GJT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAPHARMA FACTOR X KIT?

DIAPHARMA FACTOR X KIT is a medical device that received FDA 510(k) clearance on 2004-07-12. The listed applicant is Diapharma Group, Inc.. The 510(k) number is K040362.

When did DIAPHARMA FACTOR X KIT receive FDA 510(k) clearance?

DIAPHARMA FACTOR X KIT received FDA 510(k) clearance on 2004-07-12, under 510(k) number K040362.

Who is the listed applicant for DIAPHARMA FACTOR X KIT?

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

What is the FDA product code for DIAPHARMA FACTOR X KIT?

The FDA product code for DIAPHARMA FACTOR X KIT is GJT.

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: GJT)

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.

K222831CRYOcheck Factor VIII Deficient Plasma with VWFPrecision Biologic, Inc.K180486HemosIL Factor XII Deficient PlasmaInstrumentation Laboratory COK102851NOFACT VIIIR2 Diagnostics, Inc.K102908NOFACT IXR2 Diagnostics, Inc.K110237HEMOSIL FACTOR VIII DEFICIENT PLASMAInstrumentation Laboratory COK050661HEMOSIL FACTOR II DEFICIENT PLASMAInstrumentation Laboratory CO

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.

↑