FUJIFILM Endoscope Model EG-740N
K-Number: K182836 · 2019-04-02
Device Summary
Frequently Asked Questions
What is the FUJIFILM Endoscope Model EG-740N?
FUJIFILM Endoscope Model EG-740N is a medical device that received FDA 510(k) clearance on 2019-04-02. The listed applicant is Fujifilm Corporation. The 510(k) number is K182836.
When did FUJIFILM Endoscope Model EG-740N receive FDA 510(k) clearance?
FUJIFILM Endoscope Model EG-740N received FDA 510(k) clearance on 2019-04-02, under 510(k) number K182836.
Who is the listed applicant for FUJIFILM Endoscope Model EG-740N?
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 FUJIFILM Endoscope Model EG-740N?
The FDA product code for FUJIFILM Endoscope Model EG-740N is FDS.
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: FDS)
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.