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FDA 510(k)

PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES

K-Number: K941750 · 1994-11-01

ApplicantBoston Scientific Corp
Decision Date1994-11-01
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1994-11-01 under 510(k) number K941750. 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 PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES?

PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES is a medical device that received FDA 510(k) clearance on 1994-11-01. The listed applicant is Boston Scientific Corp. The 510(k) number is K941750.

When did PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES receive FDA 510(k) clearance?

PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES received FDA 510(k) clearance on 1994-11-01, under 510(k) number K941750.

Who is the listed applicant for PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES?

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

What is the FDA product code for PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES?

The FDA product code for PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES is FDI.

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Other records listing Boston Scientific Corp 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.

K243245IceSeed 1.5 CX Straight Needle (H7493968333170); IceSphere1.5 CX Straight Needle (H7493968435730); IceRod 1.5 CX Straight Needle (H7493968535330)K231328LUX-Dx II (M302); LUX-Dx II+ (M312)K133566ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM WITH THE PERIPHERAL ROTALINK PLUSK133208INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEMK131700SENSATION SHORT THROW, CAPTIFLEX, CAPTIVATOR, CAPTIVATOR II, PROFILE, SINGLE-USE POLYPECTOMY SNARESK131914OFFROAD RE-ENTRY CATHETER SYSTEM

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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.

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