FDA 510(k)

MICOR Lens Fragmentation System

N.º K: K214028 · 2022-09-09

SolicitanteCarl Zeiss Meditec Cataract Technology, Inc.

Fecha de decisión2022-09-09

Código de productoHQC

Comité asesorOP

DecisiónSubstantially Equivalent

Resumen del dispositivo

MICOR Lens Fragmentation System is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss Meditec Cataract Technology, Inc.. It received FDA 510(k) clearance on 2022-09-09 under 510(k) number K214028. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

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. The listed applicant is Carl Zeiss Meditec Cataract Technology, Inc.. The 510(k) number is K214028.

When did MICOR Lens Fragmentation System receive FDA 510(k) clearance?

MICOR Lens Fragmentation System received FDA 510(k) clearance on 2022-09-09, under 510(k) number K214028.

Who is the listed applicant for MICOR Lens Fragmentation System?

The FDA 510(k) record lists Carl Zeiss Meditec Cataract Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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Otros registros que enlistan a Carl Zeiss Meditec Cataract Technology, Inc. como solicitante

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)K222236miCOR System Lens Fragmentation System K200207xPORT S Lens Fragmentation System K200584xPORT 304 (miCOR) System Lens Fragmentation System K191024xPORT Lens Fragmentation System

Ver todos los 7 dispositivos →

Dispositivos relacionados (Código: HQC)

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Fuente oficial

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