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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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