The following data is part of a premarket notification filed by Vas-cath, Inc. with the FDA for Opti-plast 7f Peripheral Angioplasty Catheter.
| Device ID | K902367 |
| 510k Number | K902367 |
| Device Name: | OPTI-PLAST 7F PERIPHERAL ANGIOPLASTY CATHETER |
| Classification | Catheter, Angioplasty, Peripheral, Transluminal |
| Applicant | VAS-CATH, INC. 2380 TEDLO ST. Mississauga, Ontario, CA L5a 3v3 |
| Contact | Guillen, Eng |
| Correspondent | Guillen, Eng VAS-CATH, INC. 2380 TEDLO ST. Mississauga, Ontario, CA L5a 3v3 |
| Product Code | LIT |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-05-29 |
| Decision Date | 1990-12-03 |