The following data is part of a premarket notification filed by Chiron Vision Corp. with the FDA for Modification To The Site Peristaltic Module System.
| Device ID | K883199 |
| 510k Number | K883199 |
| Device Name: | MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM |
| Classification | Unit, Phacofragmentation |
| Applicant | CHIRON VISION CORP. 135 GIBRALTAR RD. Horsham, PA 19044 |
| Contact | James Mccracken |
| Correspondent | James Mccracken CHIRON VISION CORP. 135 GIBRALTAR RD. Horsham, PA 19044 |
| Product Code | HQC |
| CFR Regulation Number | 886.4670 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-07-28 |
| Decision Date | 1988-09-15 |