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FDA 510(k)

HEMORRHOIDAL LIGATION INSTR. SYSTEM

K-Number: K801352 · 1980-07-08

ApplicantDepuy, Inc.
Decision Date1980-07-08
Product CodeFHN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HEMORRHOIDAL LIGATION INSTR. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1980-07-08 under 510(k) number K801352. 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 HEMORRHOIDAL LIGATION INSTR. SYSTEM?

HEMORRHOIDAL LIGATION INSTR. SYSTEM is a medical device that received FDA 510(k) clearance on 1980-07-08. The listed applicant is Depuy, Inc.. The 510(k) number is K801352.

When did HEMORRHOIDAL LIGATION INSTR. SYSTEM receive FDA 510(k) clearance?

HEMORRHOIDAL LIGATION INSTR. SYSTEM received FDA 510(k) clearance on 1980-07-08, under 510(k) number K801352.

Who is the listed applicant for HEMORRHOIDAL LIGATION INSTR. SYSTEM?

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

What is the FDA product code for HEMORRHOIDAL LIGATION INSTR. SYSTEM?

The FDA product code for HEMORRHOIDAL LIGATION INSTR. SYSTEM is FHN.

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Other records listing Depuy, Inc. as applicant

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K043058PINNACLE CONSTRAINED ACETABULAR LINERSK042664LPS UPPER EXTREMITYK041085LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARYK033959LPSK040544DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062K021478DELTA SHOULDER

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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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