FDA 510(k) Applications Submitted by WINDY HILL TECHNOLOGY, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K993342 10/05/1999 DUCPREP BREAST ASPIRATOR, MODEL PMPO2 WINDY HILL TECHNOLOGY, INC.
K983867 11/02/1998 FUJI CATHETER, MODEL CTH001 WINDY HILL TECHNOLOGY, INC.


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