The following data is part of a premarket notification filed by Coopervision, Inc. with the FDA for Kcp Pak Convenience Pack.
Device ID | K850148 |
510k Number | K850148 |
Device Name: | KCP PAK CONVENIENCE PACK |
Classification | Unit, Phacofragmentation |
Applicant | COOPERVISION, INC. 17701 COWAN AVE.P. O. BOX 19587 Irvine, CA 92713 |
Contact | David W Drapp |
Correspondent | David W Drapp COOPERVISION, INC. 17701 COWAN AVE.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 | 1985-01-14 |
Decision Date | 1985-04-15 |