Atlas FDA

Visumax; VISUMAX 800

FDA premarket approval P150040/S021 · decided 2025-08-21

Approval details

PMA number
P150040
Supplement
S021
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Visumax; VISUMAX 800
Generic name
Femtosecond laser system for refractive correction
Applicant
Carl Zeiss Meditec, Inc.
Date received
2025-07-25
Decision date
2025-08-21
Days to decision
27 days
Decision code
OK30
Product code
OTL
Advisory committee
Ophthalmic
Expedited review
No
Location
Dublin, CA
Statement
approval of a new supplier for the slider component of the OPMI arm of the VISUMAX 800 Femtosecond Laser

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510(k) clearances by this applicant

RecordFirmDate
CLARUS (700) (K243878)Carl Zeiss Meditec, Inc.2025-04-17
CIRRUS™ HD-OCT Model 6000 (K233933)Carl Zeiss Meditec, Inc.2024-05-17
VISULAS yag (K230350)Carl Zeiss Meditec, Inc.2023-09-22
Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option) (K231075)Carl Zeiss Meditec, Inc.2023-06-20
CIRRUS HD-OCT (K222200)Carl Zeiss Meditec, Inc.2023-04-13
CLARUS (K191194)Carl Zeiss Meditec, Inc.2019-06-25
CIRRUS HD-OCT (K181534)Carl Zeiss Meditec, Inc.2019-02-15
CLARUS (K181444)Carl Zeiss Meditec, Inc.2019-01-10