VISULAS combi
K-Number: K233911 · 2024-09-06
ApplicantCarl Zeiss Meditec, AG
Decision Date2024-09-06
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
VISULAS combi is a medical device manufactured by Carl Zeiss Meditec, AG. It received FDA 510(k) clearance on 2024-09-06 under approval number K233911. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VISULAS combi?
VISULAS combi is a medical device that received FDA 510(k) clearance on 2024-09-06. It is manufactured by Carl Zeiss Meditec, AG. The 510(k) number is K233911.
When was VISULAS combi approved by the FDA?
VISULAS combi received FDA 510(k) clearance on 2024-09-06, under approval number K233911.
What company makes VISULAS combi?
VISULAS combi is manufactured by Carl Zeiss Meditec, AG.
What is the FDA product code for VISULAS combi?
The FDA product code for VISULAS combi is HQF.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.