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FDA 510(k)

NEXUS HEMORRHOID LIGATOR

K-Number: K131282 · 2013-07-11

ApplicantInx Medical
Decision Date2013-07-11
Product CodeFHN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEXUS HEMORRHOID LIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Inx Medical. It received FDA 510(k) clearance on 2013-07-11 under 510(k) number K131282. The device is classified under product code FHN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEXUS HEMORRHOID LIGATOR?

NEXUS HEMORRHOID LIGATOR is a medical device that received FDA 510(k) clearance on 2013-07-11. The listed applicant is Inx Medical. The 510(k) number is K131282.

When did NEXUS HEMORRHOID LIGATOR receive FDA 510(k) clearance?

NEXUS HEMORRHOID LIGATOR received FDA 510(k) clearance on 2013-07-11, under 510(k) number K131282.

Who is the listed applicant for NEXUS HEMORRHOID LIGATOR?

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

What is the FDA product code for NEXUS HEMORRHOID LIGATOR?

The FDA product code for NEXUS HEMORRHOID LIGATOR is FHN.

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Related Devices (Code: FHN)

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.

K213223Multi-Band LigatorBeijing Zksk Technology Co., Ltd.K172985Ligation DeviceLeo Medical Co., Ltd.K093497THD BANDYThd SpaK091519HAEMOBAND MULTI-LIGATORHaemoband Surgical, Ltd.K070881LEM HEMORRHOIDAL LIGATOR, MODELS A.5650, A.5660Sapimed S.P.A.K020824SPEEDBAND SUPERVIEW SUPER 7, INJECTION SPEEDBAND SUPERVIEW SUPER 7, MODELS 4205 AND 4238Boston Scientific Corp

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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