FDA 510(k) Applications Submitted by MICHAEL G PRICE

FDA 510(k) Number Submission Date Device Name Applicant
K050847 04/04/2005 IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206A THERATECH, INC.
K060975 04/10/2006 IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2 THERATECH, INC.
K993934 11/18/1999 V QUICK PATCH VQ CORP.
K024090 12/11/2002 NYLON SUTURE AUROLAB
K024091 12/11/2002 SILK SUTURES AUROLAB


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