IRIX: Receives FDA 510(k) Clearance for IQ Laser Systems
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Submitted By Knobias ClipReport
By Fain Hughes, fhughes@knobias.com
IRIDEX Corporation (IRIX) announced receipt of FDA 510(k) clearance for its Family of IRIDEX IQ Laser Systems. This clearance covers the IRIDEX IQ 532, IQ 577, IQ 630-670, and IQ 810 Laser Systems and their associated delivery devices to deliver laser energy in either CW-Pulse(TM), MicroPulse(TM) or LongPulse(TM) mode. These Laser Systems are intended for a wide range of specific applications in the medical specialties of ophthalmology, ear, nose and throat (ENT)/otolaryngology and dermatology.
