The following data is part of a premarket notification filed by Cyden Limited with the FDA for Ifl Professional System, Model C100.
Device ID | K040156 |
510k Number | K040156 |
Device Name: | IFL PROFESSIONAL SYSTEM, MODEL C100 |
Classification | Powered Laser Surgical Instrument |
Applicant | CYDEN LIMITED TECHNIUM, KINGS ROAD THE DOCKS Swansea, Wales, GB Sa1 8ph |
Contact | Michael Noel Kiernan |
Correspondent | Michael Noel Kiernan CYDEN LIMITED TECHNIUM, KINGS ROAD THE DOCKS Swansea, Wales, GB Sa1 8ph |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-01-23 |
Decision Date | 2004-03-24 |
Summary: | summary |