Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

“MoFi” Cell Culture Basal Medium

K-Number: K240247 · 2024-07-12

Decision Date2024-07-12
Product CodeNDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

“MoFi” Cell Culture Basal Medium is a medical device manufactured by Duogenic Stemcells Corporation. It received FDA 510(k) clearance on 2024-07-12 under approval number K240247. 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 “MoFi” Cell Culture Basal Medium?

“MoFi” Cell Culture Basal Medium is a medical device that received FDA 510(k) clearance on 2024-07-12. It is manufactured by Duogenic Stemcells Corporation. The 510(k) number is K240247.

When was “MoFi” Cell Culture Basal Medium approved by the FDA?

“MoFi” Cell Culture Basal Medium received FDA 510(k) clearance on 2024-07-12, under approval number K240247.

What company makes “MoFi” Cell Culture Basal Medium?

“MoFi” Cell Culture Basal Medium is manufactured by Duogenic Stemcells Corporation.

What is the FDA product code for “MoFi” Cell Culture Basal Medium?

The FDA product code for “MoFi” Cell Culture Basal Medium is NDS.

Related Clinical Trials

Related Devices (Code: NDS)

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.