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FDA 510(k) Applications Submitted by IMPAX TECHNOLOGY, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K993532
10/19/1999
DDS, DS3000, RS3000, CS5000, OT3000, IS3000, RS5000, CD3000, US3000, (AMONGST OTHER NAMES)
IMPAX TECHNOLOGY, INC.
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