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FDA 510(k)

3d Cage

K-Number: K180347 · 2019-10-28

ApplicantFims Co., Ltd.
Decision Date2019-10-28
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

3d Cage is the device name listed in this FDA 510(k) record. The listed applicant is Fims Co., Ltd.. It received FDA 510(k) clearance on 2019-10-28 under 510(k) number K180347. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3d Cage?

3d Cage is a medical device that received FDA 510(k) clearance on 2019-10-28. The listed applicant is Fims Co., Ltd.. The 510(k) number is K180347.

When did 3d Cage receive FDA 510(k) clearance?

3d Cage received FDA 510(k) clearance on 2019-10-28, under 510(k) number K180347.

Who is the listed applicant for 3d Cage?

The FDA 510(k) record lists Fims Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3d Cage?

The FDA product code for 3d Cage is MAX.

Other records listing Fims Co., Ltd. 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.

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Related Devices (Code: MAX)

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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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