FDA 510(k) clearance · back to tracker

Solo Scope Colonoscope System

Gi View, Ltd. cleared K261015 on 2026-08-21, decision: substantially equivalent

K-number

K261015

Sponsor

Gi View, Ltd.

Device

Solo Scope Colonoscope System

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-08-21

Product code

FDF

Advisory committee

Gastroenterology, Urology

Medical specialty

Gastroenterology, Urology

Regulation number

876.1500

Official FDA record

Open K261015on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.