Atlas FDA

ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM

FDA 510(k) clearance K023249 · decided 2002-10-18

Clearance details

K-number
K023249
Device name
ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM
Applicant
Alcon Laboratories, Inc.
Decision
Substantially Equivalent
Date received
2002-09-30
Decision date
2002-10-18
Days to decision
18 days
Clearance type
Abbreviated
Product code
NCF
Device class
1
Regulation number
886.1760
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Orlando, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM (K062930)Alcon Research, Ltd.2006-11-08
OPD-STATION SOFTWARE (K050336)Nidek, Inc.2005-08-24
CUSTOMCORNEA MEASUREMENT DEVICE (CCMD) (K000637)Alcon Laboratories, Inc.2000-05-19

Recalls involving this device

RecordFirmDate
''Alcon Ladarwave CustomCornea Wavefront System'' Aberrometer software Version 7.91 recall (Z-1078-03)Alcon Laboratories, Inc.2003-08-06

PMA approvals by this applicant

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