FDA 510(k)

KARL STORZ TIPCAM1 Rubina

N.º K: K262547 · 2026-09-21

Fecha de decisión2026-09-21

Código de productoOWN

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

KARL STORZ TIPCAM1 Rubina is the device name listed in this FDA 510(k) record. The listed applicant is KALR STORZ SE & Co. KG. It received FDA 510(k) clearance on 2026-09-21 under 510(k) number K262547. The device is classified under product code OWN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the KARL STORZ TIPCAM1 Rubina?

KARL STORZ TIPCAM1 Rubina is a medical device that received FDA 510(k) clearance on 2026-09-21. The listed applicant is KALR STORZ SE & Co. KG. The 510(k) number is K262547.

When did KARL STORZ TIPCAM1 Rubina receive FDA 510(k) clearance?

KARL STORZ TIPCAM1 Rubina received FDA 510(k) clearance on 2026-09-21, under 510(k) number K262547.

¿Quién es el solicitante registrado para KARL STORZ TIPCAM1 Rubina?

The FDA 510(k) record lists KALR STORZ SE & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KARL STORZ TIPCAM1 Rubina?

The FDA product code for KARL STORZ TIPCAM1 Rubina is OWN.

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Fuente oficial

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