FDA 510(k) Applications Submitted by JENNIFER MARS

FDA 510(k) Number Submission Date Device Name Applicant
K040764 03/25/2004 STRYKER T4 HYTREL ZIPPER TOGA STRYKER CORP.
K042405 09/03/2004 PAINPUMP1; PAINPUMP2 STRYKER CORP.
K043466 12/15/2004 PAINPUMP2 STRYKER INSTRUMENTS


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