FDA 510(k) Applications Submitted by HEIDI MASTEN

FDA 510(k) Number Submission Date Device Name Applicant
K013241 09/28/2001 ARNDT EMERGENCY CRICOTHYROTOMY CATHETER SET COOK, INC.
K013252 09/28/2001 PATIL EMERGENCY CRICOTHYROTOMY CATHETER SET COOK, INC.
K013916 11/27/2001 MELKER EMERGENCY CRICOTHYROTOMY CATHETER SET COOK, INC.


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