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FDA 510(k)

EZ-SCOPE AN, EZ-SCOPE LIGHT

K-Number: K022342 · 2002-10-09

Decision Date2002-10-09
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EZ-SCOPE AN, EZ-SCOPE LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Anzai Medical Co., Ltd.. It received FDA 510(k) clearance on 2002-10-09 under 510(k) number K022342. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ-SCOPE AN, EZ-SCOPE LIGHT?

EZ-SCOPE AN, EZ-SCOPE LIGHT is a medical device that received FDA 510(k) clearance on 2002-10-09. The listed applicant is Anzai Medical Co., Ltd.. The 510(k) number is K022342.

When did EZ-SCOPE AN, EZ-SCOPE LIGHT receive FDA 510(k) clearance?

EZ-SCOPE AN, EZ-SCOPE LIGHT received FDA 510(k) clearance on 2002-10-09, under 510(k) number K022342.

Who is the listed applicant for EZ-SCOPE AN, EZ-SCOPE LIGHT?

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

What is the FDA product code for EZ-SCOPE AN, EZ-SCOPE LIGHT?

The FDA product code for EZ-SCOPE AN, EZ-SCOPE LIGHT is IYX.

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.

Other records listing Anzai Medical Co., 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.

Related Devices (Code: IYX)

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.

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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