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Blade Works, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K020079BLADEWORKS MICROKERATOME BLADE, MODEL 7061April 19, 2002
K993225BLADEWORKS MICROKERATOME BLADEMarch 20, 2000
K993591BLADEWORKS DISPOSABLE ALK TUBINGDecember 28, 1999