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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 the device name listed in this FDA 510(k) record. The listed applicant is Ybrain, Inc.. It received FDA 510(k) clearance on 2024-06-11 under 510(k) 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. The listed applicant is Ybrain, Inc.. The 510(k) number is K232749.

When did DOOPANG receive FDA 510(k) clearance?

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

Who is the listed applicant for DOOPANG?

The FDA 510(k) record lists Ybrain, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOOPANG?

The FDA product code for DOOPANG is PCC.

Related Devices (Code: PCC)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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