ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm)
N.º K: K163529 · 2017-03-29
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Resumen del dispositivo
Preguntas frecuentes
What is the ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm)?
ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm) is a medical device that received FDA 510(k) clearance on 2017-03-29. The listed applicant is Avery Dennison Corporation. The 510(k) number is K163529.
When did ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm) receive FDA 510(k) clearance?
ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm) received FDA 510(k) clearance on 2017-03-29, under 510(k) number K163529.
Who is the listed applicant for ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm)?
The FDA 510(k) record lists Avery Dennison Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm)?
The FDA product code for ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm) is FRO. This falls under the Anesthesiology category.
Ensayos clínicos relacionados
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Dispositivos relacionados (Código: FRO)
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.
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