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FDA 510(k)

OLYMPUS MEASURING DEVICES

K-Number: K933717 · 1993-11-02

ApplicantOlympus Corp.
Decision Date1993-11-02
Product CodeFDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS MEASURING DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1993-11-02 under 510(k) number K933717. The device is classified under product code FDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS MEASURING DEVICES?

OLYMPUS MEASURING DEVICES is a medical device that received FDA 510(k) clearance on 1993-11-02. The listed applicant is Olympus Corp.. The 510(k) number is K933717.

When did OLYMPUS MEASURING DEVICES receive FDA 510(k) clearance?

OLYMPUS MEASURING DEVICES received FDA 510(k) clearance on 1993-11-02, under 510(k) number K933717.

Who is the listed applicant for OLYMPUS MEASURING DEVICES?

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 MEASURING DEVICES?

The FDA product code for OLYMPUS MEASURING DEVICES is FDS.

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: FDS)

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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