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FDA 510(k)

miCOR System Lens Fragmentation System

K-Number: K222236 · 2022-08-24

ApplicantCarl Zeiss Meditec Cataract Technology, Inc.
Decision Date2022-08-24
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

miCOR System Lens Fragmentation System is a medical device manufactured by Carl Zeiss Meditec Cataract Technology, Inc.. It received FDA 510(k) clearance on 2022-08-24 under approval number K222236. 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 System Lens Fragmentation System?

miCOR System Lens Fragmentation System is a medical device that received FDA 510(k) clearance on 2022-08-24. It is manufactured by Carl Zeiss Meditec Cataract Technology, Inc.. The 510(k) number is K222236.

When was miCOR System Lens Fragmentation System approved by the FDA?

miCOR System Lens Fragmentation System received FDA 510(k) clearance on 2022-08-24, under approval number K222236.

What company makes miCOR System Lens Fragmentation System?

miCOR System Lens Fragmentation System is manufactured by Carl Zeiss Meditec Cataract Technology, Inc..

What is the FDA product code for miCOR System Lens Fragmentation System?

The FDA product code for miCOR System Lens Fragmentation System is HQC.

Related Clinical Trials

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Other Devices by Carl Zeiss Meditec Cataract Technology, Inc.

K191024xPORT Lens Fragmentation System K200207xPORT S Lens Fragmentation System K200584xPORT 304 (miCOR) System Lens Fragmentation System K214028MICOR Lens Fragmentation System K243395MICOR 700 with Auto I/A K242801MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185)

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Related Devices (Code: 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.

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