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FDA 510(k) Applications Submitted by DIANE DAVIS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K961122
03/21/1996
STRYKER KNIFELIGHT
STRYKER INSTRUMENTS
K961970
05/20/1996
COMMAND 2 MICOELECTRIC SURGICAL SYSTEM
STRYKER CORP.
K962800
07/18/1996
STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES
STRYKER INSTRUMENTS
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