LASIK EXPOSED

LASIK manufacturers and their collaborators successfully pressured FDA to classify these problems as mere “symptoms” so that manufacturers could claim that the adverse event rate is less than one percent. MORRIS WAXLER

Monday, January 27, 2014

Nidek EC-5000 Excimer Laser System - P970053/S009

http://www.accessdata.fda.gov/cdrh_docs/pdf/P970053S009c.pdf



MEL 80™ Excimer Laser System - P060004

http://www.accessdata.fda.gov/cdrh_docs/pdf6/P060004d.pdf







WaveLight ALLEGRETTO WAVE™ Excimer Laser System - P020050/S004

http://www.accessdata.fda.gov/cdrh_docs/pdf2/P020050S004d.pdf




LADARVision® 4000 Excimer Laser System and the LADAR™ 6000 Excimer Laser System - P970043/S022

http://www.accessdata.fda.gov/cdrh_docs/pdf/P970043S022d.pdf





LADARVision® 4000 Excimer Laser System and the LADAR™ 6000 Excimer Laser System - P970043/S022

http://www.accessdata.fda.gov/cdrh_docs/pdf/P970043S020d.pdf








WaveLight ALLEGRETTO WAVE™ Excimer Laser System - P030008/S004

http://www.accessdata.fda.gov/cdrh_docs/pdf3/P030008S004d.pdf




Summary Information on: STAR S4 IR™ Excimer Laser System with Variable Spot Scanning (VSS™) and WaveScan WaveFront® System - P930016/S021

http://www.accessdata.fda.gov/cdrh_docs/pdf/P930016S021b.pdf


STAR S4 IR™ Excimer Laser System with Variable Spot Scanning (VSS™) and WaveScan WaveFront® System - P930016/S020

http://www.accessdata.fda.gov/cdrh_docs/pdf/P930016S020b.pdf













Posted by Lasik Investigation at 5:02 AM
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