The following data is part of a premarket notification filed by Dayton Mfg. Co. with the FDA for Summit Optics Soft Contact Lens Case.
Device ID | K870164 |
510k Number | K870164 |
Device Name: | SUMMIT OPTICS SOFT CONTACT LENS CASE |
Classification | Case, Contact Lens |
Applicant | DAYTON MFG. CO. P.O. BOX 271504 Tampa, FL 33624 |
Contact | Michael P Dayton,ma |
Correspondent | Michael P Dayton,ma DAYTON MFG. CO. P.O. BOX 271504 Tampa, FL 33624 |
Product Code | LRX |
CFR Regulation Number | 886.5928 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-01-14 |
Decision Date | 1987-02-10 |