FDA 510(k) Applications Submitted by EBI ELECTRO BIOLOGY

FDA 510(k) Number Submission Date Device Name Applicant
K973683 09/26/1997 OMEGA 21 SYSTEM EBI ELECTRO BIOLOGY
K973923 10/15/1997 EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM EBI ELECTRO BIOLOGY
K991721 05/20/1999 EBI OMEGA 21 SYSTEM EBI ELECTRO BIOLOGY


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