The following data is part of a premarket notification filed by Coopervision, Inc. with the FDA for Coopervision System Vi.
Device ID | K842945 |
510k Number | K842945 |
Device Name: | COOPERVISION SYSTEM VI |
Classification | Unit, Phacofragmentation |
Applicant | COOPERVISION, INC. P.O. BOX 19587 Irvine , CA 92713 - |
Contact | Douglas G Allen |
Correspondent | Douglas G Allen COOPERVISION, INC. P.O. BOX 19587 Irvine , CA 92713 - |
Product Code | HQC |
CFR Regulation Number | 886.4670 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-07-25 |
Decision Date | 1984-12-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
COOPERVISION SYSTEM VI 73518041 1384136 Dead/Cancelled |
COOPERVISION, INC. 1985-01-18 |