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FDA 510(k)

HAEMOBAND MULTI-LIGATOR

K-Number: K091519 · 2009-07-28

ApplicantHaemoband Surgical, Ltd.
Decision Date2009-07-28
Product CodeFHN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HAEMOBAND MULTI-LIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Haemoband Surgical, Ltd.. It received FDA 510(k) clearance on 2009-07-28 under 510(k) number K091519. 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 HAEMOBAND MULTI-LIGATOR?

HAEMOBAND MULTI-LIGATOR is a medical device that received FDA 510(k) clearance on 2009-07-28. The listed applicant is Haemoband Surgical, Ltd.. The 510(k) number is K091519.

When did HAEMOBAND MULTI-LIGATOR receive FDA 510(k) clearance?

HAEMOBAND MULTI-LIGATOR received FDA 510(k) clearance on 2009-07-28, under 510(k) number K091519.

Who is the listed applicant for HAEMOBAND MULTI-LIGATOR?

The FDA 510(k) record lists Haemoband Surgical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAEMOBAND MULTI-LIGATOR?

The FDA product code for HAEMOBAND MULTI-LIGATOR is FHN.

Related Clinical Trials

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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Other records listing Haemoband Surgical, Ltd. 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.

K250645SleeveLUX 24 Anoscope/Proctoscope (P2001); SleeveLUX 16 Anoscope/Proctoscope (P2002)

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.K131282NEXUS HEMORRHOID LIGATORInx MedicalK093497THD BANDYThd SpaK070881LEM 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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