Atlas FDA

MODIFIED J & C LOOP POSTERIOR CHAMBER SINGLE PIECE

FDA premarket approval P880072/S019 · decided 1992-01-17

Approval details

PMA number
P880072
Supplement
S019
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
MODIFIED J & C LOOP POSTERIOR CHAMBER SINGLE PIECE
Generic name
intraocular lens
Applicant
Eyekon Medical, Inc.
Date received
1991-02-19
Decision date
1992-01-17
Days to decision
332 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Clearwater, FL

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
Temporary Keratoprosthesis (QuickSet TKP™) (K261312)Eyekon Medical, Inc.2026-07-24