The following data is part of a premarket notification filed by U.s. Iol, Inc. with the FDA for Phaco Tip.
Device ID | K954746 |
510k Number | K954746 |
Device Name: | PHACO TIP |
Classification | Unit, Phacofragmentation |
Applicant | U.S. IOL, INC. 9327 BLACKLEY ST. Temple City, CA 91789 |
Contact | Glen A Dunki-jacobs |
Correspondent | Glen A Dunki-jacobs U.S. IOL, INC. 9327 BLACKLEY ST. Temple City, CA 91789 |
Product Code | HQC |
CFR Regulation Number | 886.4670 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-10-16 |
Decision Date | 1996-01-11 |