Atlas FDA

TECNIS ACRYLIC IOLS

FDA premarket approval P990080/S025 · decided 2007-07-10

Approval details

PMA number
P990080
Supplement
S025
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
TECNIS ACRYLIC IOLS
Generic name
intraocular lens
Applicant
Johnson & Johnson Surgical Vision, Inc.
Date received
2007-06-13
Decision date
2007-07-10
Days to decision
27 days
Decision code
OK30
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Irvine, CA
Statement
REDUCTION OF THE TOTAL PROCESS TIME.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
ELITA™ Femtosecond Laser System, ELITA™ Patient Interface (K223566)Johnson & Johnson Surgical Vision, Inc.2023-04-14
VERITAS Phacoemulsification Console, VERITAS Advanced Fluidics Pack and Advanced Infusion Pack, VERITAS Swivel Handpiece, VERITAS Advanced Foot Pedal, VERITAS Remote Control (K203060)Johnson & Johnson Surgical Vision, Inc.2021-03-12
UNFOLDER Vitan Inserter (K191949)Johnson & Johnson Surgical Vision, Inc.2019-09-13
COMPACT INTUITIV System, COMPACT INTUITIV Wireless Remote Control, COMPACT INTUITIV Four-Button Foot Pedal, COMPACT INTUITIV Closed-Toe Foot Pedal (K191933)Johnson & Johnson Surgical Vision, Inc.2019-08-16