The following data is part of a premarket notification filed by Cavitron Corp. with the FDA for Cavitron Ultrasonic Surg. Aspir. Cusa.
| Device ID | K801623 |
| 510k Number | K801623 |
| Device Name: | CAVITRON ULTRASONIC SURG. ASPIR. CUSA |
| Classification | Instrument, Ultrasonic Surgical |
| Applicant | CAVITRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LFL |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-07-15 |
| Decision Date | 1980-11-18 |