FDA 510(k) Applications Submitted by SELICOR, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K020227 01/22/2002 SELICOR, MODELS A100 & D100 SELICOR, INC.
K030382 02/05/2003 SELITHERM, MODEL C100 SELICOR, INC.


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