The following data is part of a premarket notification filed by Al.chi.mi.a with the FDA for Eusol-c.
Device ID | K063617 |
510k Number | K063617 |
Device Name: | EUSOL-C |
Classification | Media, Corneal Storage |
Applicant | AL.CHI.MI.A 377 ROUTE 17 S Hasbrouck Heights, NJ 07604 |
Contact | George Myers |
Correspondent | George Myers AL.CHI.MI.A 377 ROUTE 17 S Hasbrouck Heights, NJ 07604 |
Product Code | LYX |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-12-05 |
Decision Date | 2007-02-08 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EUSOL-C 97613897 not registered Live/Pending |
Oftalone, Inc 2022-09-30 |