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FDA 510(k) Applications Submitted by JONATHAN WOODWARD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030891
03/21/2003
SURGISTAR MICROKERATOME BLADE, MODEL NO. 2400-LSK
SURGISTAR, INC.
K961524
04/22/1996
STERILAB CANNULAS, STERILAB CYSTOTMES, STERILAB NEEDLES AND STERILAB LENS MANIPULATORS
STERILAB, INC.
K992978
09/03/1999
RICROKERATOME BLADE
SURGISTAR, INC.
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