Class Class II
FUJIFILM Endoscope Model EI-740D/S (K221551)
Description
FUJIFILM Endoscope Model EI-740D/S by Fujifilm Corporaton, an FDA 510(k) cleared gastroenterology, urology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK221551
Clearance Date2023-01-27
Clearance TypeTraditional
Product CodeFDS
Regulation Number876.1500
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K221551
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. FUJIFILM Endoscope Model EI-740D/S (K221551) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K210162 | Endoscope Model EI-740D/S | Fujifilm Corporation | 2021 |
Trace the full predicate network for K221551
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.