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

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

FDA 510(k) Number	Applicant	Device Name	Decision Date
K965070	MECTA CORP.	SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.	03/06/1997
K960754	MECTA CORP.	SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M	09/18/1996
K192834	Mecta Corporation	MECTA Sigma	04/26/2020

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