FDA 510(k)

CROMA Electrosurgical Generator (PRD-EMR-050)

N.º K: K242983 · 2025-02-05

Fecha de decisión2025-02-05

Código de productoGEI

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

CROMA Electrosurgical Generator (PRD-EMR-050) is the device name listed in this FDA 510(k) record. The listed applicant is Creo Medical, Ltd.. It received FDA 510(k) clearance on 2025-02-05 under 510(k) number K242983. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CROMA Electrosurgical Generator (PRD-EMR-050)?

CROMA Electrosurgical Generator (PRD-EMR-050) is a medical device that received FDA 510(k) clearance on 2025-02-05. The listed applicant is Creo Medical, Ltd.. The 510(k) number is K242983.

When did CROMA Electrosurgical Generator (PRD-EMR-050) receive FDA 510(k) clearance?

CROMA Electrosurgical Generator (PRD-EMR-050) received FDA 510(k) clearance on 2025-02-05, under 510(k) number K242983.

Who is the listed applicant for CROMA Electrosurgical Generator (PRD-EMR-050)?

The FDA 510(k) record lists Creo Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CROMA Electrosurgical Generator (PRD-EMR-050)?

The FDA product code for CROMA Electrosurgical Generator (PRD-EMR-050) is GEI.

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Otros registros que enlistan a Creo Medical, Ltd. como solicitante

K242774SpydrBlade Flex Instrument (PRD-RG1-001)K242061Reusable Interface Cable 1.5 m (PRD-IFC-002)K230328Speedboat Flush SB1 Instrument K223138Instrumento Electrosurgical AB1, Sistema Electrosurgical Creo K221672Creo Electrosurgical System with NP1 Instrument K200298ABI Instrumento, Sistema Electrosurgical Creo

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Fuente oficial

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