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FDA 510(k)

DOOPANG

K-Number: K232749 · 2024-06-11

ApplicantYbrain, Inc.
Decision Date2024-06-11
Product CodePCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DOOPANG is a medical device manufactured by Ybrain, Inc.. It received FDA 510(k) clearance on 2024-06-11 under approval number K232749. The device is classified under product code PCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOOPANG?

DOOPANG is a medical device that received FDA 510(k) clearance on 2024-06-11. It is manufactured by Ybrain, Inc.. The 510(k) number is K232749.

When was DOOPANG approved by the FDA?

DOOPANG received FDA 510(k) clearance on 2024-06-11, under approval number K232749.

What company makes DOOPANG?

DOOPANG is manufactured by Ybrain, Inc..

What is the FDA product code for DOOPANG?

The FDA product code for DOOPANG is PCC.

Related Devices (Code: PCC)

Official Source

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