FDA 510(k) Applications Submitted by BLADE WORKS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K993591 10/22/1999 BLADEWORKS DISPOSABLE ALK TUBING BLADE WORKS, INC.
K993225 09/27/1999 BLADEWORKS MICROKERATOME BLADE BLADE WORKS, INC.
K020079 01/10/2002 BLADEWORKS MICROKERATOME BLADE, MODEL 7061 BLADE WORKS, INC.


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