FDA 510(k) Applications Submitted by CURBELL ELECTRONICS INC.

FDA 510(k) Number Submission Date Device Name Applicant
K081762 06/20/2008 CURBELL PATIENT MONITORING CABLES CURBELL ELECTRONICS INC.
K080605 03/04/2008 SURE-LOCK ELECTRODE CLIP, MODEL CL-34, CL-A60, CL-HW, CL-TL CURBELL ELECTRONICS INC.


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