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FDA 510(k)

MSC SFM

K-Number: K232543 · 2024-09-06

ApplicantYocon Biology Technology Company
Decision Date2024-09-06
Product CodeNDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MSC SFM is the device name listed in this FDA 510(k) record. The listed applicant is Yocon Biology Technology Company. It received FDA 510(k) clearance on 2024-09-06 under 510(k) number K232543. The device is classified under product code NDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSC SFM?

MSC SFM is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Yocon Biology Technology Company. The 510(k) number is K232543.

When did MSC SFM receive FDA 510(k) clearance?

MSC SFM received FDA 510(k) clearance on 2024-09-06, under 510(k) number K232543.

Who is the listed applicant for MSC SFM?

The FDA 510(k) record lists Yocon Biology Technology Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MSC SFM?

The FDA product code for MSC SFM is NDS.

Related Devices (Code: NDS)

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

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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