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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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