QUATERA 700
K-Number: K230858 · 2023-07-31
ApplicantCarl Zeiss Meditec, AG
Decision Date2023-07-31
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
QUATERA 700 is a medical device manufactured by Carl Zeiss Meditec, AG. It received FDA 510(k) clearance on 2023-07-31 under approval number K230858. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the QUATERA 700?
QUATERA 700 is a medical device that received FDA 510(k) clearance on 2023-07-31. It is manufactured by Carl Zeiss Meditec, AG. The 510(k) number is K230858.
When was QUATERA 700 approved by the FDA?
QUATERA 700 received FDA 510(k) clearance on 2023-07-31, under approval number K230858.
What company makes QUATERA 700?
QUATERA 700 is manufactured by Carl Zeiss Meditec, AG.
What is the FDA product code for QUATERA 700?
The FDA product code for QUATERA 700 is HQC.
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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.