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POSTERIOR CHAMBER INTROCULAR LENSES

FDA premarket approval P830056/S075 · decided 1996-04-02

Approval details

PMA number
P830056
Supplement
S075
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
POSTERIOR CHAMBER INTROCULAR LENSES
Generic name
intraocular lens
Applicant
Carl Zeiss Meditec, AG
Date received
1994-06-17
Decision date
1996-04-02
Days to decision
655 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Dublin, CA
Statement
APPROVAL FOR MODELS C420P, C540U, C445F, C840U, U240F0, C540MC, U211F, AND U241FO POSTERIOR CHAMBER INTRAOCULAR LENSES AS TIER A MODIFICATIONS OF CLINICALLY STUDIED PARTENT LENSES

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510(k) clearances by this applicant

RecordFirmDate
ZEISS CLINIC 360 (K260694)Carl Zeiss Meditec, AG2026-07-17
INTRABEAM (700); And accessories (INTRABEAM SMART Stand, INTRABEAM SMART Spherical Applicator, INTRABEAM Spherical Sizer Set, INTRABEAM Needle Applicator) (K241174)Carl Zeiss Meditec, AG2025-01-10
VISULAS combi (K233911)Carl Zeiss Meditec, AG2024-09-06
BLUE 400; BLUE 400 S (K240215)Carl Zeiss Meditec, AG2024-06-28
RESCAN 700 (K233421)Carl Zeiss Meditec, AG2024-03-08
CALLISTO eye (K232944)Carl Zeiss Meditec, AG2023-12-21
QEVO System (K232159)Carl Zeiss Meditec, AG2023-09-21
CALLISTO eye (K231676)Carl Zeiss Meditec, AG2023-08-28