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FDA 510(k)

GIP/MEID-GLOBE HOT BIOPSY FORCEPS

K-Number: K953355 · 1996-04-04

ApplicantMedi-Globe Corp.
Decision Date1996-04-04
Product CodeKGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GIP/MEID-GLOBE HOT BIOPSY FORCEPS 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 1996-04-04 under 510(k) number K953355. The device is classified under product code KGE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GIP/MEID-GLOBE HOT BIOPSY FORCEPS?

GIP/MEID-GLOBE HOT BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1996-04-04. The listed applicant is Medi-Globe Corp.. The 510(k) number is K953355.

When did GIP/MEID-GLOBE HOT BIOPSY FORCEPS receive FDA 510(k) clearance?

GIP/MEID-GLOBE HOT BIOPSY FORCEPS received FDA 510(k) clearance on 1996-04-04, under 510(k) number K953355.

Who is the listed applicant for GIP/MEID-GLOBE HOT BIOPSY FORCEPS?

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/MEID-GLOBE HOT BIOPSY FORCEPS?

The FDA product code for GIP/MEID-GLOBE HOT BIOPSY FORCEPS is KGE.

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Other records listing Medi-Globe Corp. as applicant

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K061222INJECTRA INJECTION NEEDLEK051247SONOTIP II ULTRASOUND NEEDLE SYSTEMK011261STONE EXTRACTOR BALLOON CATHETERK010714EXPANDER, MODELS 1400880, 1401280, 1401680, 1401880, 1410420, 1410620, 1410830K010549BILIARY AND PANCREATIC ENDOPROSTHESES (STENTS)K990220MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM

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Related Devices (Code: KGE)

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.

K251807Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LROlympus Medical Systems Corp.K250187Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U)Olympus Medical Systems CorporationK242857ClearHemograsperFinemedix Co., Ltd.K231721Disposable Hot Biopsy ForcepsBeijing Zksk Technology Co., Ltd.K220053Diathermic Slitter (FlushKnife) DK2620JI and DK2623JIFujifilm CorporationK210406Bipolar Coagulation ForecepsHangzhou AGS MedTech 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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