FDA 510(k)

Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set

N.º K: K182832 · 2019-06-26

Fecha de decisión2019-06-26

Código de productoKGC

Comité asesorGU

DecisiónUnknown

Resumen del dispositivo

Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set is the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2019-06-26 under 510(k) number K182832. The device is classified under product code KGC. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Preguntas frecuentes

What is the Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set?

Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set is a medical device that received FDA 510(k) clearance on 2019-06-26. The listed applicant is Cook Incorporated. The 510(k) number is K182832.

When did Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set receive FDA 510(k) clearance?

Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set received FDA 510(k) clearance on 2019-06-26, under 510(k) number K182832.

Who is the listed applicant for Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set?

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

What is the FDA product code for Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set?

The FDA product code for Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set is KGC.

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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.