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FDA 510(k)

ETHICON ENDO SURGERY ARTICULATING SNARE

K-Number: K073288 · 2008-06-12

ApplicantEthicon Endo-Surgery, Inc.
Decision Date2008-06-12
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ETHICON ENDO SURGERY ARTICULATING SNARE is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, Inc.. It received FDA 510(k) clearance on 2008-06-12 under 510(k) number K073288. 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 ETHICON ENDO SURGERY ARTICULATING SNARE?

ETHICON ENDO SURGERY ARTICULATING SNARE is a medical device that received FDA 510(k) clearance on 2008-06-12. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K073288.

When did ETHICON ENDO SURGERY ARTICULATING SNARE receive FDA 510(k) clearance?

ETHICON ENDO SURGERY ARTICULATING SNARE received FDA 510(k) clearance on 2008-06-12, under 510(k) number K073288.

Who is the listed applicant for ETHICON ENDO SURGERY ARTICULATING SNARE?

The FDA 510(k) record lists Ethicon Endo-Surgery, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ETHICON ENDO SURGERY ARTICULATING SNARE?

The FDA product code for ETHICON ENDO SURGERY ARTICULATING SNARE is FDI.

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Other records listing Ethicon Endo-Surgery, 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.

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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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