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FDA 510(k)

FORUM

K-Number: K213527 · 2022-08-15

ApplicantCarl Zeiss Meditec, AG
Decision Date2022-08-15
Product CodeNFJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FORUM is a medical device manufactured by Carl Zeiss Meditec, AG. It received FDA 510(k) clearance on 2022-08-15 under approval number K213527. 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 FORUM?

FORUM is a medical device that received FDA 510(k) clearance on 2022-08-15. It is manufactured by Carl Zeiss Meditec, AG. The 510(k) number is K213527.

When was FORUM approved by the FDA?

FORUM received FDA 510(k) clearance on 2022-08-15, under approval number K213527.

What company makes FORUM?

FORUM is manufactured by Carl Zeiss Meditec, AG.

What is the FDA product code for FORUM?

The FDA product code for FORUM is 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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