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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