FDA 510(k) Application Details - K202699

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K202699
Device Name	Anesthesia Conduction Kit
Applicant	PAJUNK GmbH Medizintechnologie Karl-Hall-Str 1 Geisingen 78187 DE Other 510(k) Applications for this Company
Contact	Christian G.H. Quass Other 510(k) Applications for this Contact
Regulation Number	868.5140   More FDA Info for this Regulation Number
Classification Product Code	CAZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/16/2020
Decision Date	12/29/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review