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FDA 510(k)

LAPAROSCOPIC SNARE

K-Number: K911482 · 1991-04-22

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1991-04-22
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC SNARE is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1991-04-22 under 510(k) number K911482. 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 LAPAROSCOPIC SNARE?

LAPAROSCOPIC SNARE is a medical device that received FDA 510(k) clearance on 1991-04-22. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K911482.

When did LAPAROSCOPIC SNARE receive FDA 510(k) clearance?

LAPAROSCOPIC SNARE received FDA 510(k) clearance on 1991-04-22, under 510(k) number K911482.

Who is the listed applicant for LAPAROSCOPIC SNARE?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPIC SNARE?

The FDA product code for LAPAROSCOPIC SNARE is FDI.

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Other records listing United States Endoscopy Group, Inc. as applicant

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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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