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FDA 510(k) Application Details - K240772
Device Classification Name
Powder, Porcelain
More FDA Info for this Device
510(K) Number
K240772
Device Name
Powder, Porcelain
Applicant
Hunan Ceramaster Material Technology Co., Ltd
103, Building B4, Dreamworks, No.1 Lantian North Road,
Xingsha Industrial Base
Changsha 410137 CN
Other 510(k) Applications for this Company
Contact
Bin Wang
Other 510(k) Applications for this Contact
Regulation Number
872.6660
More FDA Info for this Regulation Number
Classification Product Code
EIH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/21/2024
Decision Date
05/20/2024
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
FDA Source Information for K240772
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