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)

SNARE,FLEXIBLE

K-Number: K002927 · 2000-12-10

ApplicantOdon Lifetechnology
Decision Date2000-12-10
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SNARE,FLEXIBLE is the device name listed in this FDA 510(k) record. The listed applicant is Odon Lifetechnology. It received FDA 510(k) clearance on 2000-12-10 under 510(k) number K002927. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNARE,FLEXIBLE?

SNARE,FLEXIBLE is a medical device that received FDA 510(k) clearance on 2000-12-10. The listed applicant is Odon Lifetechnology. The 510(k) number is K002927.

When did SNARE,FLEXIBLE receive FDA 510(k) clearance?

SNARE,FLEXIBLE received FDA 510(k) clearance on 2000-12-10, under 510(k) number K002927.

Who is the listed applicant for SNARE,FLEXIBLE?

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

What is the FDA product code for SNARE,FLEXIBLE?

The FDA product code for SNARE,FLEXIBLE is FDI.

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: FDI)

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.

K251692Advanced Tissue Resection DeviceMicro-Tech (Nanjing) Co., Ltd.K221713Polypectomy SnareHangzhou AGS MedTech Co., Ltd.K220846CORE-SNAREIncore Co., Ltd.K220089Disposable Polyp SnareJiangsu Vedkang Medical Science and Technology Co., Ltd.K220790Disposable Polypectomy Snare, Disposable Polypectomy Hybrid SnareYangzhou Fartley Medical Instrument Technology Co., Ltd.K213222Disposable Polypectomy SnareBeijing Zksk Technology Co., Ltd.

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.

↑