FDA 510(k) Applications Submitted by TENS CARE LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K020846 03/15/2002 ULTIMA TENS XL-A1 TENS CARE LTD.
K003591 11/21/2000 TENSCARE, MODEL TENS XL-2 TENS CARE LTD.
K011543 05/18/2001 TENS CARE, MODEL XL-Y3 TENS CARE LTD.


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