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FDA 510(k)

Nanum Syringe

K-Number: K201930 · 2021-01-17

Decision Date2021-01-17
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Nanum Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Nanum Company Co., Ltd.. It received FDA 510(k) clearance on 2021-01-17 under 510(k) number K201930. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nanum Syringe?

Nanum Syringe is a medical device that received FDA 510(k) clearance on 2021-01-17. The listed applicant is Nanum Company Co., Ltd.. The 510(k) number is K201930.

When did Nanum Syringe receive FDA 510(k) clearance?

Nanum Syringe received FDA 510(k) clearance on 2021-01-17, under 510(k) number K201930.

Who is the listed applicant for Nanum Syringe?

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

What is the FDA product code for Nanum Syringe?

The FDA product code for Nanum Syringe is FMF.

Related Devices (Code: FMF)

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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