FDA 510(k) Applications Submitted by INTERNATIONAL REGULATORY CONSULTANTS

FDA 510(k) Number Submission Date Device Name Applicant
K981591 05/04/1998 VORTEK URETERAL DOUBLE LOOP STENT, BIOSOFT URETERAL DOUBLE LOOP STENT INTERNATIONAL REGULATORY CONSULTANTS
K971347 04/10/1997 MEDISURF INTERNATIONAL REGULATORY CONSULTANTS
K962614 07/03/1996 SHIFA STERILE DISPOSABLE SYRINGES INTERNATIONAL REGULATORY CONSULTANTS


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