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FDA 510(k)

F&P 950 Accessory Breathing Circuit Kits

N.º K: K221436 · 2023-06-29

SolicitanteFisher & Paykel Healthcare, Ltd.
Fecha de decisión2023-06-29
Código de productoBZD
Comité asesorAN
DecisiónSubstantially Equivalent

Resumen del dispositivo

F&P 950 Accessory Breathing Circuit Kits is the device name listed in this FDA 510(k) record. The listed applicant is Fisher & Paykel Healthcare, Ltd.. It received FDA 510(k) clearance on 2023-06-29 under 510(k) number K221436. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the F&P 950 Accessory Breathing Circuit Kits?

F&P 950 Accessory Breathing Circuit Kits is a medical device that received FDA 510(k) clearance on 2023-06-29. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K221436.

When did F&P 950 Accessory Breathing Circuit Kits receive FDA 510(k) clearance?

F&P 950 Accessory Breathing Circuit Kits received FDA 510(k) clearance on 2023-06-29, under 510(k) number K221436.

Who is the listed applicant for F&P 950 Accessory Breathing Circuit Kits?

The FDA 510(k) record lists Fisher & Paykel Healthcare, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for F&P 950 Accessory Breathing Circuit Kits?

The FDA product code for F&P 950 Accessory Breathing Circuit Kits is BZD.

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Dispositivos relacionados (Código: BZD)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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Fuente oficial

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