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FDA 510(k)

OLYMPUS HX-20 SERIES LIGATING DEVICE

K-Number: K984255 · 1999-01-12

ApplicantOlympus Corp of America
Decision Date1999-01-12
Product CodeMND
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS HX-20 SERIES LIGATING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp of America. It received FDA 510(k) clearance on 1999-01-12 under 510(k) number K984255. The device is classified under product code MND. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS HX-20 SERIES LIGATING DEVICE?

OLYMPUS HX-20 SERIES LIGATING DEVICE is a medical device that received FDA 510(k) clearance on 1999-01-12. The listed applicant is Olympus Corp of America. The 510(k) number is K984255.

When did OLYMPUS HX-20 SERIES LIGATING DEVICE receive FDA 510(k) clearance?

OLYMPUS HX-20 SERIES LIGATING DEVICE received FDA 510(k) clearance on 1999-01-12, under 510(k) number K984255.

Who is the listed applicant for OLYMPUS HX-20 SERIES LIGATING DEVICE?

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

What is the FDA product code for OLYMPUS HX-20 SERIES LIGATING DEVICE?

The FDA product code for OLYMPUS HX-20 SERIES LIGATING DEVICE is MND.

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 Olympus Corp of America 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.

K944250UREA NITROGEN REAGENT

Related Devices (Code: MND)

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.

K132535AUTOBAND LIGATOREndochoice, Inc.K083556MODIFICATION TO AUTO-BAND LIGATORScandimed InternationalK081142AUTO-BAND LIGATORScandimed InternationalK051950INSCOPE MULTI-CLIP APPLIER, MODELS IN22321, IN23321Ethicon Endo-Surgery, Inc.K031236AUTO-BAND LIGATORScandimed. A.S.K033245BARD ULTRAVIEW MULTIPLE BAND LIGATOR, MODEL 00700UC.R. Bard, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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