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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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