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)

EN SNARE ENDOVASCULAR SNARE SYSTEM

K-Number: K092343 · 2009-08-07

ApplicantMerit Medical Systems, Inc.
Decision Date2009-08-07
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EN SNARE ENDOVASCULAR SNARE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2009-08-07 under 510(k) number K092343. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EN SNARE ENDOVASCULAR SNARE SYSTEM?

EN SNARE ENDOVASCULAR SNARE SYSTEM is a medical device that received FDA 510(k) clearance on 2009-08-07. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K092343.

When did EN SNARE ENDOVASCULAR SNARE SYSTEM receive FDA 510(k) clearance?

EN SNARE ENDOVASCULAR SNARE SYSTEM received FDA 510(k) clearance on 2009-08-07, under 510(k) number K092343.

Who is the listed applicant for EN SNARE ENDOVASCULAR SNARE SYSTEM?

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

What is the FDA product code for EN SNARE ENDOVASCULAR SNARE SYSTEM?

The FDA product code for EN SNARE ENDOVASCULAR SNARE SYSTEM is MMX.

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 Merit Medical Systems, Inc. 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.

K261310FlexTract Deflectable-Rotational Dilator Sheath SetK262086PreludeSYNC™ Radial Compression DeviceK254073StatSeal DiscK251802STAR RF Ablation SystemK252892SCOUT MD Surgical Guidance SystemK250853Merit Syringe

View all 159 devices →

Related Devices (Code: MMX)

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.

K242776LimFlow V-CeiverLimFlow, Inc.K241259Amplatz Goose Neck Snare KitMedtronic, Inc.K232443Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval KitArgon Medical Devices, Inc.K222254Gunther Tulip Vena Cava Filter Retrieval SetCook IncorporatedK222083LimFlow V-CeiverLimFlow, Inc.K212988ONO Retrieval DeviceOnocor Vascular, LLC

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.

↑