References in periodicals archive ?
The Panel will review a PMA application for the Sunrise LTK System for the reduction of hyperopia within the range of +0.
Food and Drug Administration (FDA), to not recommend that the FDA approve the Sunrise LTK System at this time.
Food and Drug Administration (FDA) approved the HYPERION LTK System as safe and effective by for the temporary reduction of hyperopia in patients 40 years of age or older with or without astigmatism.
The increase in revenue is due to the sale of forty-eight HYPERION(TM) LTK SYSTEM units during the third quarter of 2000, which is on pace for the largest U.
The increase in revenue is due to the sale of two HYPERION(TM) LTK System units to clinical investigators during the second quarter of 2000.
Even though we are only one month into our launch, we are already closing orders at a rate of more than one HYPERION(TM) LTK System per business day," said C.
In fact, the HYPERION(TM) LTK System has been designed with input from ophthalmologists around the world.
Sunrise will release its 2nd Quarter financial results and a status report on Hyperion(TM) LTK System orders on August 9, 2000.
BW2: ( BW)(CA-SUNRISE-TECHNOLOGIES-PHOTO) ADVISORY/Photos of HYPERION(tm) LTK System and C.
The HYPERION(TM) LTK System gently heats eye tissue outside the center of the cornea, thereby causing it to steepen and reduce hyperopia (farsightedness).
Approximately 100 physicians attended the session, which featured presentations by Sunrise clinical investigators, and a demonstration of the HYPERION LTK System by R.
Food and Drug Administration (FDA) to exchange the Company's new HYPERION(TM) LTK System for the Sun 1000 Holmium Laser System at all of its clinical investigational sites.
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