EW10-EC02 Endoscopy Support Program
K-Number: K260567 · 2026-08-07
Device Summary
Frequently Asked Questions
What is the EW10-EC02 Endoscopy Support Program?
EW10-EC02 Endoscopy Support Program is a medical device that received FDA 510(k) clearance on 2026-08-07. The listed applicant is Fujifilm Corporation. The 510(k) number is K260567.
When did EW10-EC02 Endoscopy Support Program receive FDA 510(k) clearance?
EW10-EC02 Endoscopy Support Program received FDA 510(k) clearance on 2026-08-07, under 510(k) number K260567.
Who is the listed applicant for EW10-EC02 Endoscopy Support Program?
The FDA 510(k) record lists Fujifilm Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EW10-EC02 Endoscopy Support Program?
The FDA product code for EW10-EC02 Endoscopy Support Program is QNP.
Other records listing Fujifilm Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: QNP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.