The following data is part of a premarket notification filed by American Edwards Laboratories with the FDA for Angioscopy Catheter.
| Device ID | K832698 |
| 510k Number | K832698 |
| Device Name: | ANGIOSCOPY CATHETER |
| Classification | Angioscope |
| Applicant | AMERICAN EDWARDS LABORATORIES 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | LYK |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-10 |
| Decision Date | 1983-11-03 |