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FDA 510(k) Application Details - K242086
Device Classification Name
More FDA Info for this Device
510(K) Number
K242086
Device Name
MagDI System (MAG-01, DS-01)
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
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Classification Product Code
SAH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/17/2024
Decision Date
10/24/2024
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
FDA Source Information for K242086
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