Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500D
Summary
Fujifilm Corporaton received 510(k) clearance for Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500D, a FDA device. Cleared on 2023-01-11.
Details
Source
510(k) Clearance
External ID
K223295
Action Date
2023-01-11
Status
Special
Category
device
Product Code
FDA
Product Description
Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500D. Product code: FDA.
Company
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Fujifilm Corporaton has received 4 total clearances in our database.
Fujifilm Corporaton has 4 FDA actions in our database, including 4 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Fujifilm Corporaton have FDA actions?
Fujifilm Corporaton has 4 FDA actions in our database, including 0 recalls and 4 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K223295" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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