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FDA 510(k) Application Details - DEN240013
Device Classification Name
More FDA Info for this Device
510(K) Number
DEN240013
Device Name
MagDI System
Applicant
GT Metabolic Solutions, Inc.
3050 Three Springs Court
San Jose, CA 95140 US
Other 510(k) Applications for this Company
Contact
Lisa Griffin Vincent
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
SAH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/26/2024
Decision Date
07/02/2024
Decision
DENG -
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type
Post-NSE
Reviewed By Third Party
N
Expedited Review
FDA Source Information for DEN240013
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