FDA 510(k)

External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters

Número K: K242974 · 2025-06-20

Data da decisão2025-06-20

Código do produtoJXG

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters is the device name listed in this FDA 510(k) record. The listed applicant is Sophysa. It received FDA 510(k) clearance on 2025-06-20 under 510(k) number K242974. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters?

External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters is a medical device that received FDA 510(k) clearance on 2025-06-20. The listed applicant is Sophysa. The 510(k) number is K242974.

When did External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters receive FDA 510(k) clearance?

External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters received FDA 510(k) clearance on 2025-06-20, under 510(k) number K242974.

Who is the listed applicant for External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters?

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

What is the FDA product code for External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters?

The FDA product code for External CSF Drainage Ventricular Catheters, External CSF Drainage Lumbar Catheters is JXG.

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Outros registros que listam Sophysa como candidato(a)

K252241Pressio 3 Multi-parameter Neuromonitoring System K250636Sophy Mini Monopressure Valve (SM1)K222422Polaris Valve Electronic Reading Instrument

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Fonte oficial

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