FDA 510(k) Application Details - K242591

Device Classification Name	Unit, X-Ray, Extraoral With Timer   More FDA Info for this Device
510(K) Number	K242591
Device Name	Unit, X-Ray, Extraoral With Timer
Applicant	DRTECH Corporation Suite No.1, 2 Floor / Suite No. 2, 3 Floor, 29 Dunchon-Daero 541beon-gil Seongnam-si 13216 KR Other 510(k) Applications for this Company
Contact	Yeongsuk An Other 510(k) Applications for this Contact
Regulation Number	872.1800   More FDA Info for this Regulation Number
Classification Product Code	EHD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/30/2024
Decision Date	11/01/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
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