FDA 510(k) Applications Submitted by RESPIRONICS GEORGIA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K011597 05/24/2001 SMARTMONITOR 2, MODEL 4000 RESPIRONICS GEORGIA, INC.
K001708 06/05/2000 PROFOX SOFTWARE, MODEL 920M-41 RESPIRONICS GEORGIA, INC.


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