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FDA 510(k) Application Details - K212320
Device Classification Name
Negative Pressure Wound Therapy Powered Suction Pump
More FDA Info for this Device
510(K) Number
K212320
Device Name
Negative Pressure Wound Therapy Powered Suction Pump
Applicant
3M Health Care Business Group
6203 Farinon Dr.
San Antonio, TX 78249 US
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Contact
Teri Feeley
Other 510(k) Applications for this Contact
Regulation Number
878.4780
More FDA Info for this Regulation Number
Classification Product Code
OMP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/26/2021
Decision Date
09/28/2021
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
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