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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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