Atlas FDA

HYPERION LTK SYSTEM

FDA premarket approval P990078 · decided 2000-06-30

Approval details

PMA number
P990078
Trade name
HYPERION LTK SYSTEM
Generic name
Laser, neodymium:Yag, ophthalmic for uses other than posterior capsulotomy & cutting pupillary
Applicant
Sunrise Technologies, Inc.
Date received
1999-11-03
Decision date
2000-06-30
Days to decision
240 days
Decision code
APPR
Product code
LOI
Advisory committee
Ophthalmic
Expedited review
No
Location
Fremont, CA
Statement
APPROVAL FOR THE SUNRISE HYPERION(TM) LTK SYSTEM. THE DEVICE IS INDICATED FOR TEMPORARY REDUCTION OF HYPEROPIA IN PATIENTS WITH +0.75 TO +2.5 DIOPTERS OF MANIFEST REFRACTION SPHERICLA EQUIVALENT (MRSE) AT THE SPECTACLE PLANE (WITH CYLINDER LESS THAN OR EQUAL TO +-0.75 DIOPTERS) WHO ARE 40 YEARS OF AGE OR OLDER WITH DOCUMENTED STABILITY OF REFRACTION FOR THE PRIOR 6 MONTHS, AS DEMONSTRATED BY A CHANGE OF LESS THAN OR EQUAL TO 0.50D IN SPHERICAL, AND CYLINDRICAL COMPONENTS OF THE MANIFEST REFRACS

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510(k) clearances by this applicant

RecordFirmDate
SUNRISE CURING LAMP (K962192)Sunrise Technologies, Inc.1996-09-03
SLASE 210 PLUS HOLMIUM LASER SYSTEM (K942542)Sunrise Technologies, Inc.1994-09-01
MICROPREP CAVITY PREPERATION SYSTEM (K932997)Sunrise Technologies, Inc.1994-04-25
SLASE 210 & SLASE 210 PLUS HOLMIUM LASER SYSTEMS (K933007)Sunrise Technologies, Inc.1994-01-10
MODEL 5030 SUCTION HANDPIECE SYSTEM (K933017)Sunrise Technologies, Inc.1993-07-26
UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASER (K931774)Sunrise Technologies, Inc.1993-07-22
8-WATT PULSED DENTAL LASER SYSTEM (K930789)Sunrise Technologies, Inc.1993-05-21
2.5 WATT PULSED DENTAL LASER SYSTEM (K930879)Sunrise Technologies, Inc.1993-05-21