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FDA 510(k) Applications Submitted by Ortek Therapeutics, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K002989
09/25/2000
PROCLUDE
ORTEK THERAPEUTICS, INC.
K003482
11/09/2000
PROCLUDE-SENSITIVE
ORTEK THERAPEUTICS, INC.
K170822
03/20/2017
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Ortek Therapeutics, Inc.
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