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)

SLIMCATH-DX MODELS, 3SUXXXX, 3SBXXXX, AND FCXXXX

K-Number: K993698 · 2000-08-16

ApplicantMogul Enterprises
Decision Date2000-08-16
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SLIMCATH-DX MODELS, 3SUXXXX, 3SBXXXX, AND FCXXXX is the device name listed in this FDA 510(k) record. The listed applicant is Mogul Enterprises. It received FDA 510(k) clearance on 2000-08-16 under 510(k) number K993698. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLIMCATH-DX MODELS, 3SUXXXX, 3SBXXXX, AND FCXXXX?

SLIMCATH-DX MODELS, 3SUXXXX, 3SBXXXX, AND FCXXXX is a medical device that received FDA 510(k) clearance on 2000-08-16. The listed applicant is Mogul Enterprises. The 510(k) number is K993698.

When did SLIMCATH-DX MODELS, 3SUXXXX, 3SBXXXX, AND FCXXXX receive FDA 510(k) clearance?

SLIMCATH-DX MODELS, 3SUXXXX, 3SBXXXX, AND FCXXXX received FDA 510(k) clearance on 2000-08-16, under 510(k) number K993698.

Who is the listed applicant for SLIMCATH-DX MODELS, 3SUXXXX, 3SBXXXX, AND FCXXXX?

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

What is the FDA product code for SLIMCATH-DX MODELS, 3SUXXXX, 3SBXXXX, AND FCXXXX?

The FDA product code for SLIMCATH-DX MODELS, 3SUXXXX, 3SBXXXX, AND FCXXXX is DRF.

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 Mogul Enterprises 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.

K0308524 FRENCH & 5 FRENCH ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS MODELS 5UEXXX, 5BEXXX AND 5FEXXX, AND 4UEXXX, 4BEXXX AND 4FEXK0117346-FRENCH, 20-ELECTRODE ELECTROPHYSIOLOGY DIAGNOSTIC CATHETER, MODELS 6U20XXX, 6B20XXX, AND 6F20XXX

Related Devices (Code: DRF)

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.

K252794Vision-MR™ Diagnostic CatheterImricor Medical Systems, Inc.K250590MAGiC Sweep™ EP Mapping CatheterStereotaxis, Inc.K250310VIKING™ Fixed Curve Diagnostic CatheterBoston Scientific CorporationK240366EP•XT™ Unidirectional Steerable Diagnostic Catheter; Dynamic Tip™ Unidirectional Steerable Diagnostic Catheter; Dynamic XT™ Unidirectional Steerable Diagnostic CatheterBoston Scientific CorporationK233900Nordica PV Cryo Mapping CatheterSynaptic Medical CorporationK233397Cosine-10TM Diagnostic CatheterMedtronic, 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.

↑