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FDA 510(k) Application Details - K222773
Device Classification Name
More FDA Info for this Device
510(K) Number
K222773
Device Name
Feeding Tube
Applicant
Anhui Tiankang Medical Technology Co., Ltd.
No. 228, Weiyi Road, Economic Development Zone
Tianchang 239300 CN
Other 510(k) Applications for this Company
Contact
Zhang Yong
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
PIF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/14/2022
Decision Date
08/17/2023
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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