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FDA 510(k)

Retina Workplace

K-Number: K182318 · 2018-10-24

ApplicantCarl Zeiss Meditec, Inc.
Decision Date2018-10-24
Product CodeNFJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Retina Workplace is a medical device manufactured by Carl Zeiss Meditec, Inc.. It received FDA 510(k) clearance on 2018-10-24 under approval number K182318. The device is classified under product code NFJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Retina Workplace?

Retina Workplace is a medical device that received FDA 510(k) clearance on 2018-10-24. It is manufactured by Carl Zeiss Meditec, Inc.. The 510(k) number is K182318.

When was Retina Workplace approved by the FDA?

Retina Workplace received FDA 510(k) clearance on 2018-10-24, under approval number K182318.

What company makes Retina Workplace?

Retina Workplace is manufactured by Carl Zeiss Meditec, Inc..

What is the FDA product code for Retina Workplace?

The FDA product code for Retina Workplace is NFJ.

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Related Devices (Code: NFJ)

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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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