Atlas FDA

HEALON(R) VISCOELASTIC PRODUCTS

FDA premarket approval P810031/S019 · decided 1995-05-03

Approval details

PMA number
P810031
Supplement
S019
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
HEALON(R) VISCOELASTIC PRODUCTS
Generic name
AID, SURGICAL, VISCOELASTIC
Applicant
Johnson & Johnson Surgical Vision, Inc.
Date received
1994-10-07
Decision date
1995-05-03
Days to decision
208 days
Decision code
APPR
Product code
LZP
Advisory committee
Ophthalmic
Expedited review
No
Location
Irvine, CA

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