FDA 510(k) Application Details - K214002

Device Classification Name	Test, Qualitative And Quantitative Factor Deficiency   More FDA Info for this Device
510(K) Number	K214002
Device Name	Test, Qualitative And Quantitative Factor Deficiency
Applicant	Precision BioLogic Inc. 140 Eileen Stubbs Avenue Dartmouth B3B 0A9 CA Other 510(k) Applications for this Company
Contact	Karen Black Other 510(k) Applications for this Contact
Regulation Number	864.7290   More FDA Info for this Regulation Number
Classification Product Code	GGP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/21/2021
Decision Date	12/23/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	HE - Hematology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review