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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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