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FDA 510(k)

VIRTUAL SLIDE SYSTEM, OLYMPUS VS800 SYSTEM

K-Number: K111914 · 2012-08-21

ApplicantOlympus America Inc. / Scientific Equipment Group
Decision Date2012-08-21
Product CodeOEO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VIRTUAL SLIDE SYSTEM, OLYMPUS VS800 SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Olympus America Inc. / Scientific Equipment Group. It received FDA 510(k) clearance on 2012-08-21 under 510(k) number K111914. The device is classified under product code OEO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIRTUAL SLIDE SYSTEM, OLYMPUS VS800 SYSTEM?

VIRTUAL SLIDE SYSTEM, OLYMPUS VS800 SYSTEM is a medical device that received FDA 510(k) clearance on 2012-08-21. The listed applicant is Olympus America Inc. / Scientific Equipment Group. The 510(k) number is K111914.

When did VIRTUAL SLIDE SYSTEM, OLYMPUS VS800 SYSTEM receive FDA 510(k) clearance?

VIRTUAL SLIDE SYSTEM, OLYMPUS VS800 SYSTEM received FDA 510(k) clearance on 2012-08-21, under 510(k) number K111914.

Who is the listed applicant for VIRTUAL SLIDE SYSTEM, OLYMPUS VS800 SYSTEM?

The FDA 510(k) record lists Olympus America Inc. / Scientific Equipment Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIRTUAL SLIDE SYSTEM, OLYMPUS VS800 SYSTEM?

The FDA product code for VIRTUAL SLIDE SYSTEM, OLYMPUS VS800 SYSTEM is OEO.

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Related Devices (Code: OEO)

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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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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