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VISULAS 690S AND VISULINK PDT/U ADAPTER

FDA premarket approval P990048/S001 · decided 2001-09-27

Approval details

PMA number
P990048
Supplement
S001
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
VISULAS 690S AND VISULINK PDT/U ADAPTER
Generic name
System, laser, photodynamic therapy
Applicant
Carl Zeiss Meditec, AG
Date received
2000-08-14
Decision date
2001-09-27
Days to decision
409 days
Decision code
APPR
Product code
MVF
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Dublin, CA
Statement
APPROVAL FOR A REVISION OF THE INDICATION FOR USE STATEMENT TO READ "FOR THE TREATMENT OF PATIENTS WITH PREDOMINANTLY CLASSIC SUBFOVEAL CHOROIDAL NEOVASCULARIZATION DUE TO MACULAR DEGENERATION, PRESUMED OCULAR HISTOPLASMOSIS, OR PATHOLOGIC MYOPIA."

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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