Atlas FDA

VISUMAX FEMTOSECOND LASER SYSTEM

FDA premarket approval P150040/S001 · decided 2017-02-28

Approval details

PMA number
P150040
Supplement
S001
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
VISUMAX FEMTOSECOND LASER SYSTEM
Generic name
Femtosecond laser system for refractive correction
Applicant
Carl Zeiss Meditec, Inc.
Date received
2017-01-06
Decision date
2017-02-28
Days to decision
53 days
Decision code
APPR
Product code
OTL
Advisory committee
Ophthalmic
Expedited review
No
Location
Dublin, CA
Statement
Approval for software changes.

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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