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FDA 510(k)

HORIZONS HOT BIOPSY FORCEPS

K-Number: K021706 · 2002-06-21

ApplicantHorizons Intl. Corp.
Decision Date2002-06-21
Product CodeKGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HORIZONS HOT BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Horizons Intl. Corp.. It received FDA 510(k) clearance on 2002-06-21 under 510(k) number K021706. 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 HORIZONS HOT BIOPSY FORCEPS?

HORIZONS HOT BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 2002-06-21. The listed applicant is Horizons Intl. Corp.. The 510(k) number is K021706.

When did HORIZONS HOT BIOPSY FORCEPS receive FDA 510(k) clearance?

HORIZONS HOT BIOPSY FORCEPS received FDA 510(k) clearance on 2002-06-21, under 510(k) number K021706.

Who is the listed applicant for HORIZONS HOT BIOPSY FORCEPS?

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

What is the FDA product code for HORIZONS HOT BIOPSY FORCEPS?

The FDA product code for HORIZONS HOT BIOPSY FORCEPS is KGE.

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Other records listing Horizons Intl. 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.

K083049TORNADO ROTATABEL SNARE AND POLYP CATCHERK022268HORIZONS REUSABLE POLYPECTOMY SNARESK022243HORIZONS REUSABLE HOT BIOPSY FORCEPSK022546HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLESK021998HORIZONS CYTOLOGY BRUSHK011667HORIZONS INTERNATIONAL POLYPECTOMY SNARES

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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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