The following data is part of a premarket notification filed by Chiron Vision Corp. with the FDA for Iocare Ultrasonic Titanium Tips.
Device ID | K843278 |
510k Number | K843278 |
Device Name: | IOCARE ULTRASONIC TITANIUM TIPS |
Classification | Unit, Phacofragmentation |
Applicant | CHIRON VISION CORP. 9342 JERONIMO RD. Irvine, CA 92618 -1903 |
Contact | Ticknor |
Correspondent | Ticknor CHIRON VISION CORP. 9342 JERONIMO RD. Irvine, CA 92618 -1903 |
Product Code | HQC |
CFR Regulation Number | 886.4670 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-08-20 |
Decision Date | 1984-11-27 |