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FDA 510(k)

GIP/MEDI-GLOBE POLYPECTOMY SNARES

K-Number: K943935 · 1995-05-26

ApplicantMedi-Globe Corp.
Decision Date1995-05-26
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GIP/MEDI-GLOBE POLYPECTOMY SNARES is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Globe Corp.. It received FDA 510(k) clearance on 1995-05-26 under 510(k) number K943935. 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 GIP/MEDI-GLOBE POLYPECTOMY SNARES?

GIP/MEDI-GLOBE POLYPECTOMY SNARES is a medical device that received FDA 510(k) clearance on 1995-05-26. The listed applicant is Medi-Globe Corp.. The 510(k) number is K943935.

When did GIP/MEDI-GLOBE POLYPECTOMY SNARES receive FDA 510(k) clearance?

GIP/MEDI-GLOBE POLYPECTOMY SNARES received FDA 510(k) clearance on 1995-05-26, under 510(k) number K943935.

Who is the listed applicant for GIP/MEDI-GLOBE POLYPECTOMY SNARES?

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

What is the FDA product code for GIP/MEDI-GLOBE POLYPECTOMY SNARES?

The FDA product code for GIP/MEDI-GLOBE POLYPECTOMY SNARES is FDI.

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Other records listing Medi-Globe Corp. 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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