Atlas FDA

MODEL PS50C-OUV

FDA premarket approval P880072/S035 · decided 1995-08-07

Approval details

PMA number
P880072
Supplement
S035
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
MODEL PS50C-OUV
Generic name
intraocular lens
Applicant
Eyekon Medical, Inc.
Date received
1995-07-25
Decision date
1995-08-07
Days to decision
13 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Clearwater, FL
Statement
REQUESTED APPROVAL FOR TIER A POSTERIOR CHAMBER INTRAOCULAR LENS MODEL PS50C-OUV

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510(k) clearances by this applicant

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