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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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