FDA 510(k)

SURGIMAGE SIM 1000H Fluorescence Imaging Platform

N.º K: K253181 · 2026-05-13

Fecha de decisión2026-05-13

Código de productoIZI

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

SURGIMAGE SIM 1000H Fluorescence Imaging Platform is the device name listed in this FDA 510(k) record. The listed applicant is Surgimage Corporation. It received FDA 510(k) clearance on 2026-05-13 under 510(k) number K253181. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the SURGIMAGE SIM 1000H Fluorescence Imaging Platform?

SURGIMAGE SIM 1000H Fluorescence Imaging Platform is a medical device that received FDA 510(k) clearance on 2026-05-13. The listed applicant is Surgimage Corporation. The 510(k) number is K253181.

When did SURGIMAGE SIM 1000H Fluorescence Imaging Platform receive FDA 510(k) clearance?

SURGIMAGE SIM 1000H Fluorescence Imaging Platform received FDA 510(k) clearance on 2026-05-13, under 510(k) number K253181.

Who is the listed applicant for SURGIMAGE SIM 1000H Fluorescence Imaging Platform?

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

What is the FDA product code for SURGIMAGE SIM 1000H Fluorescence Imaging Platform?

The FDA product code for SURGIMAGE SIM 1000H Fluorescence Imaging Platform is IZI.

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Dispositivos relacionados (Código: IZI)

K261037Sistema de Imagen Portátil de Mano 780 nm SPY (SPY-PHI)Stryker Endoscopy K243645IC-Flow™ Imaging System 2.0Diagnostic Green GmbH K243077Affirm 800Digital Surgery Systems, Inc. (D.B.A True Digital Surgery)K231986Modus IRSynaptive Medical, Inc.K234090EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)Surgvision GmbH K231075Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option)Carl Zeiss Meditec, Inc.

Fuente oficial

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