The following data is part of a premarket notification filed by United Surgical Corp. with the FDA for Phacotron Day Pak.
| Device ID | K870671 |
| 510k Number | K870671 |
| Device Name: | PHACOTRON DAY PAK |
| Classification | Unit, Phacofragmentation |
| Applicant | UNITED SURGICAL CORP. 15500-A ROCKFIELD BLVD. Irvine, CA 92718 |
| Contact | Terry F Herbeck |
| Correspondent | Terry F Herbeck UNITED SURGICAL CORP. 15500-A ROCKFIELD BLVD. Irvine, CA 92718 |
| Product Code | HQC |
| CFR Regulation Number | 886.4670 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-02-19 |
| Decision Date | 1987-04-06 |