510(k) K250900

Device
EvoEndo Single-Use Endoscopy System
Applicant
EvoEndo, Inc.
510(k) number
K250900
Product code
FDS
Decision
Substantially Equivalent (SESE)
Decision date
2025-06-16
Date received
2025-03-25
Regulation
876.1500
Classification name
Gastroscope And Accessories, Flexible/Rigid
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Paul Imaoka
Address
888 E. Belvidere Rd. Suite 212 Grayslake IL US 60030 60030

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code FDS

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K250296Disposable Distal Attachment D-201 SeriesOlympus Medical Systems Corp.2025-05-01
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