Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

FDA 510(k)

Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process Indicators

N.º K: K153540 · 2016-08-04

Fecha de decisión2016-08-04
Código de productoFRG
Comité asesorHO
DecisiónSubstantially Equivalent

Resumen del dispositivo

Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process Indicators is the device name listed in this FDA 510(k) record. The listed applicant is Safe Secure Packaging Co., Ltd.. It received FDA 510(k) clearance on 2016-08-04 under 510(k) number K153540. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process Indicators?

Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process Indicators is a medical device that received FDA 510(k) clearance on 2016-08-04. The listed applicant is Safe Secure Packaging Co., Ltd.. The 510(k) number is K153540.

When did Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process Indicators receive FDA 510(k) clearance?

Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process Indicators received FDA 510(k) clearance on 2016-08-04, under 510(k) number K153540.

Who is the listed applicant for Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process Indicators?

The FDA 510(k) record lists Safe Secure Packaging Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process Indicators?

The FDA product code for Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process Indicators is FRG.

Ensayos clínicos relacionados

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.

Dispositivos relacionados (Código: FRG)

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.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

↑