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FDA 510(k) Application Details - K230131
Device Classification Name
Tubes, Gastrointestinal (And Accessories)
More FDA Info for this Device
510(K) Number
K230131
Device Name
Tubes, Gastrointestinal (And Accessories)
Applicant
ReShape Lifesciences
1001 Calle Amanecer
San Clemente, CA 92673 US
Other 510(k) Applications for this Company
Contact
Dov Gal
Other 510(k) Applications for this Contact
Regulation Number
876.5980
More FDA Info for this Regulation Number
Classification Product Code
KNT
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/17/2023
Decision Date
02/15/2023
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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