The following data is part of a premarket notification filed by Intermedics Intraocular, Inc. with the FDA for Ocucare Ultrasound Tip & Freedom Pack.
| Device ID | K834543 |
| 510k Number | K834543 |
| Device Name: | OCUCARE ULTRASOUND TIP & FREEDOM PACK |
| Classification | Unit, Phacofragmentation |
| Applicant | INTERMEDICS INTRAOCULAR, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HQC |
| CFR Regulation Number | 886.4670 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-08 |
| Decision Date | 1984-03-16 |