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)

DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998

K-Number: K091355 · 2009-07-22

ApplicantConmed Endoscopic Technologies, Inc.
Decision Date2009-07-22
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998 is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Endoscopic Technologies, Inc.. It received FDA 510(k) clearance on 2009-07-22 under 510(k) number K091355. 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 DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998?

DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998 is a medical device that received FDA 510(k) clearance on 2009-07-22. The listed applicant is Conmed Endoscopic Technologies, Inc.. The 510(k) number is K091355.

When did DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998 receive FDA 510(k) clearance?

DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998 received FDA 510(k) clearance on 2009-07-22, under 510(k) number K091355.

Who is the listed applicant for DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998?

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

What is the FDA product code for DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998?

The FDA product code for DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998 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

Other records listing Conmed Endoscopic Technologies, 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.

K080946CONMED AXCESS PAPILLOTOME MODELS AX4535, AX4535FX

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.

↑