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FDA 510(k)

MARK 5 NUVO LITE OCSI AND STD

K-Number: K082566 · 2008-12-03

Decision Date2008-12-03
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MARK 5 NUVO LITE OCSI AND STD is the device name listed in this FDA 510(k) record. The listed applicant is Nidek Medical Products, Inc.. It received FDA 510(k) clearance on 2008-12-03 under 510(k) number K082566. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARK 5 NUVO LITE OCSI AND STD?

MARK 5 NUVO LITE OCSI AND STD is a medical device that received FDA 510(k) clearance on 2008-12-03. The listed applicant is Nidek Medical Products, Inc.. The 510(k) number is K082566.

When did MARK 5 NUVO LITE OCSI AND STD receive FDA 510(k) clearance?

MARK 5 NUVO LITE OCSI AND STD received FDA 510(k) clearance on 2008-12-03, under 510(k) number K082566.

Who is the listed applicant for MARK 5 NUVO LITE OCSI AND STD?

The FDA 510(k) record lists Nidek Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARK 5 NUVO LITE OCSI AND STD?

The FDA product code for MARK 5 NUVO LITE OCSI AND STD is CAW.

Other records listing Nidek Medical Products, Inc. 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 12 devices →

Related Devices (Code: CAW)

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

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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