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FDA 510(k)

Led Mask Platinum Md

K-Number: K222377 · 2022-11-03

ApplicantCellreturn Co., Ltd.
Decision Date2022-11-03
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Led Mask Platinum Md is the device name listed in this FDA 510(k) record. The listed applicant is Cellreturn Co., Ltd.. It received FDA 510(k) clearance on 2022-11-03 under 510(k) number K222377. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Led Mask Platinum Md?

Led Mask Platinum Md is a medical device that received FDA 510(k) clearance on 2022-11-03. The listed applicant is Cellreturn Co., Ltd.. The 510(k) number is K222377.

When did Led Mask Platinum Md receive FDA 510(k) clearance?

Led Mask Platinum Md received FDA 510(k) clearance on 2022-11-03, under 510(k) number K222377.

Who is the listed applicant for Led Mask Platinum Md?

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

What is the FDA product code for Led Mask Platinum Md?

The FDA product code for Led Mask Platinum Md is OHS.

Related Devices (Code: OHS)

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

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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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