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FDA 510(k)

SUCTION-HEMORRHOID-LIGATOR

K-Number: K832192 · 1983-12-27

ApplicantResearch Endoscope Systems Intl.
Decision Date1983-12-27
Product CodeFHN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SUCTION-HEMORRHOID-LIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Research Endoscope Systems Intl.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K832192. 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 SUCTION-HEMORRHOID-LIGATOR?

SUCTION-HEMORRHOID-LIGATOR is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Research Endoscope Systems Intl.. The 510(k) number is K832192.

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

SUCTION-HEMORRHOID-LIGATOR received FDA 510(k) clearance on 1983-12-27, under 510(k) number K832192.

Who is the listed applicant for SUCTION-HEMORRHOID-LIGATOR?

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

What is the FDA product code for SUCTION-HEMORRHOID-LIGATOR?

The FDA product code for SUCTION-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.K131282NEXUS HEMORRHOID LIGATORInx MedicalK093497THD BANDYThd SpaK091519HAEMOBAND MULTI-LIGATORHaemoband Surgical, Ltd.K070881LEM HEMORRHOIDAL LIGATOR, MODELS A.5650, A.5660Sapimed S.P.A.

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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