Atlas FDA

HYPERION LTK SYSTEM

FDA premarket approval P990078/S001 · decided 2000-12-11

Approval details

PMA number
P990078
Supplement
S001
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
HYPERION LTK SYSTEM
Generic name
Laser, ophthalmic
Applicant
Sunrise Technologies, Inc.
Date received
2000-11-09
Decision date
2000-12-11
Days to decision
32 days
Decision code
APPR
Product code
HQF
Advisory committee
Ophthalmic
Expedited review
No
Location
Fremont, CA
Statement
APPROVAL FOR A CHANGE IN THE WARNING SECTION OF THE LABELING.

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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