The following data is part of a premarket notification filed by American Edwards Laboratories with the FDA for Hybrid Peripheral Dilation Catheter.
| Device ID | K834220 |
| 510k Number | K834220 |
| Device Name: | HYBRID PERIPHERAL DILATION CATHETER |
| Classification | Catheter, Angioplasty, Peripheral, Transluminal |
| Applicant | AMERICAN EDWARDS LABORATORIES 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | LIT |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-05 |
| Decision Date | 1984-01-27 |