FDA 510(k) Application Details - K203316

Device Classification Name	Negative Pressure Wound Therapy Powered Suction Pump   More FDA Info for this Device
510(K) Number	K203316
Device Name	Negative Pressure Wound Therapy Powered Suction Pump
Applicant	KCI, a part of 3M Health Care Business Group 6203 Farinon Drive San Antonio, TX 78249 US Other 510(k) Applications for this Company
Contact	Margaret Marsh 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	11/10/2020
Decision Date	10/27/2021
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