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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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