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FDA 510(k)

Metapaste Plus

K-Number: K210904 · 2021-06-30

Decision Date2021-06-30
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Metapaste Plus is the device name listed in this FDA 510(k) record. The listed applicant is Meta Biomed Co., Ltd.. It received FDA 510(k) clearance on 2021-06-30 under 510(k) number K210904. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Metapaste Plus?

Metapaste Plus is a medical device that received FDA 510(k) clearance on 2021-06-30. The listed applicant is Meta Biomed Co., Ltd.. The 510(k) number is K210904.

When did Metapaste Plus receive FDA 510(k) clearance?

Metapaste Plus received FDA 510(k) clearance on 2021-06-30, under 510(k) number K210904.

Who is the listed applicant for Metapaste Plus?

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

What is the FDA product code for Metapaste Plus?

The FDA product code for Metapaste Plus is KIF.

Other records listing Meta Biomed 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.

View all 13 devices →

Related Devices (Code: KIF)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.