FDA 510(k) Applications Submitted by JOHN J MUNRO

FDA 510(k) Number Submission Date Device Name Applicant
K090366 02/13/2009 SPEC MODEL M-31 SOURCE PRODUCTION & EQUIPMENT CO., INC.
K023073 09/16/2002 SEED LINK IMPLANT SCIENCES CORP.
K042864 10/18/2004 IMPLANT SCIENCES CORP, MODEL HDR-4140 IMPLANT SCIENCES CORP.
K052947 10/20/2005 SOURCE PRODUCTION & EQUIPMENT CO, INC., MODEL M-19 IR-192 BRACHYTHERAPY SOURCE SOURCE PRODUCTION & EQUIPMENT CO., INC.
K983436 09/29/1998 GAMMAMED PLUS HIGH DOSE RATE REMOTE AFTERLOADING SYSTEM GAMMAMED USA


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