FDA 510(k)

“MoFi” Cell Culture Basal Medium

Numéro K : K240247 · 2024-07-12

Date de décision2024-07-12

Code produitNDS

Comité consultatifGU

DécisionSubstantially Equivalent

Résumé du dispositif

“MoFi” Cell Culture Basal Medium is the device name listed in this FDA 510(k) record. The listed applicant is Duogenic Stemcells Corporation. It received FDA 510(k) clearance on 2024-07-12 under 510(k) number K240247. The device is classified under product code NDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

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. The listed applicant is Duogenic Stemcells Corporation. The 510(k) number is K240247.

When did “MoFi” Cell Culture Basal Medium receive FDA 510(k) clearance?

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

Who is the listed applicant for “MoFi” Cell Culture Basal Medium?

The FDA 510(k) record lists Duogenic Stemcells Corporation as the applicant. This does not by itself establish the device manufacturer.

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

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

Essais cliniques associés

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Dispositifs connexes (Code : NDS)

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Source officielle

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