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

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

FDA 510(k) Number	Applicant	Device Name	Decision Date
K100015	ABBOTT MOLECULAR, INC.	VYSIS CLL FISH PROBE KIT (VYSIS LSI TP53 SPECTRUMORANGE/ATM SPECTRUMGREEN) AND LSI D135319 SPECTRUMORANGE/13Q34	08/09/2011
K962873	VYSIS	CEP 12 SPECTRUMORANGE DIRECT LABELED CHROMOSOME ENUMERATION DNA PROBE	01/13/1997