FDA 510(k) Applications for Medical Device Product Code: PCG ()

FDA 510(k) Applications for Medical Device Product Code "PCG"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K121046	KRONUS MARKET DEVELOPMENT ASSOCIATES, INC.	STEROID 21-HYDROXYLASE ANTIBODY (21-OHAB) RIA ASSAY KIT	12/20/2012
K180607	KRONUS, Inc.	Steroid 21-Hydroxylase Antibody (21-OHAb) ELISA Kit	11/23/2018