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FDA 510(k)

OLYMPUS INFANT RESECTOSCOPE AND ACCESSORIES

K-Number: K904940 · 1992-01-13

ApplicantOlympus Corp.
Decision Date1992-01-13
Product CodeFJL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS INFANT RESECTOSCOPE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1992-01-13 under 510(k) number K904940. The device is classified under product code FJL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS INFANT RESECTOSCOPE AND ACCESSORIES?

OLYMPUS INFANT RESECTOSCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1992-01-13. The listed applicant is Olympus Corp.. The 510(k) number is K904940.

When did OLYMPUS INFANT RESECTOSCOPE AND ACCESSORIES receive FDA 510(k) clearance?

OLYMPUS INFANT RESECTOSCOPE AND ACCESSORIES received FDA 510(k) clearance on 1992-01-13, under 510(k) number K904940.

Who is the listed applicant for OLYMPUS INFANT RESECTOSCOPE AND ACCESSORIES?

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

What is the FDA product code for OLYMPUS INFANT RESECTOSCOPE AND ACCESSORIES?

The FDA product code for OLYMPUS INFANT RESECTOSCOPE AND ACCESSORIES is FJL.

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 Olympus Corp. 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.

View all 142 devices →

Related Devices (Code: FJL)

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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