VISULAS green
K-Number: K181682 · 2019-03-06
ApplicantCarl Zeiss Meditec, AG
Decision Date2019-03-06
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
VISULAS green is a medical device manufactured by Carl Zeiss Meditec, AG. It received FDA 510(k) clearance on 2019-03-06 under approval number K181682. 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 green?
VISULAS green is a medical device that received FDA 510(k) clearance on 2019-03-06. It is manufactured by Carl Zeiss Meditec, AG. The 510(k) number is K181682.
When was VISULAS green approved by the FDA?
VISULAS green received FDA 510(k) clearance on 2019-03-06, under approval number K181682.
What company makes VISULAS green?
VISULAS green is manufactured by Carl Zeiss Meditec, AG.
What is the FDA product code for VISULAS green?
The FDA product code for VISULAS green 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.