FDA 510(k) Application Details - K232968

Device Classification Name Mask, Surgical

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510(K) Number K232968
Device Name Mask, Surgical
Applicant Golden Grande Corp.
No. 622-6, Guanghua Li, Xuejia Dist.
Tianan 72651 TW
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Contact Hsin Hui Tseng
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Regulation Number 878.4040

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Classification Product Code FXX
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Date Received 09/21/2023
Decision Date 06/06/2024
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review

FDA Source Information for K232968


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