MICOR Lens Fragmentation System
K-Number: K214028 · 2022-09-09
Decision Date2022-09-09
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
MICOR Lens Fragmentation System is a medical device manufactured by Carl Zeiss Meditec Cataract Technology, Inc.. It received FDA 510(k) clearance on 2022-09-09 under approval number K214028. 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 MICOR Lens Fragmentation System?
MICOR Lens Fragmentation System is a medical device that received FDA 510(k) clearance on 2022-09-09. It is manufactured by Carl Zeiss Meditec Cataract Technology, Inc.. The 510(k) number is K214028.
When was MICOR Lens Fragmentation System approved by the FDA?
MICOR Lens Fragmentation System received FDA 510(k) clearance on 2022-09-09, under approval number K214028.
What company makes MICOR Lens Fragmentation System?
MICOR Lens Fragmentation System is manufactured by Carl Zeiss Meditec Cataract Technology, Inc..
What is the FDA product code for MICOR Lens Fragmentation System?
The FDA product code for MICOR Lens Fragmentation System 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.