FDA 510(k) Applications Submitted by JENNIFER PORTUGAL

FDA 510(k) Number Submission Date Device Name Applicant
K012482 08/02/2001 STORZ MODULITH SLK LITHOTRIPTER WITH MULTIVIEW OPTION KARL STORZ ENDOSCOPY-AMERICA, INC.
K011700 06/01/2001 MODULITH SLK LITHOTRIPTER KARL STORZ ENDOSCOPY
K004037 12/28/2000 X-RAY SYSTEM XR-MX KARL STORZ ENDOSCOPY


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