FDA 510(k) Application Details - K221891

Device Classification Name	Negative Pressure Wound Therapy Powered Suction Pump   More FDA Info for this Device
510(K) Number	K221891
Device Name	Negative Pressure Wound Therapy Powered Suction Pump
Applicant	Genadyne Biotechnologies, Inc 16 Midland Ave Hicksville, NY 11801 US Other 510(k) Applications for this Company
Contact	Andrew Goh 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	06/29/2022
Decision Date	12/14/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review