FDA 510(k) Application Details - K200278

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K200278
Device Name	Instrument, Biopsy
Applicant	Praxis Medical, LLC 500 N. Willow Ave. #101 Tampa, FL 33606 US Other 510(k) Applications for this Company
Contact	John Fisher Other 510(k) Applications for this Contact
Regulation Number	876.1075   More FDA Info for this Regulation Number
Classification Product Code	KNW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/04/2020
Decision Date	03/31/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review