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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

CuratOR EX2742

FDA 510(k) source

510(k) number
K262397
Applicant
Eizo Corporation
Decision date
Sep 11, 2026
Date received
Jul 14, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
GCJ
Device type
Laparoscope, General & Plastic Surgery
Device class
Class II
Regulation
21 CFR 876.1500
Advisory committee
Gastroenterology, Urology
Statement or summary
Summary
Third party
N
Location
Hakusan, Ishikawa, JP