The following data is part of a premarket notification filed by Aries Medical, Inc. with the FDA for 40cc Percutaneous Furl Dou. Lumen Balloon Catheter.
| Device ID | K864567 |
| 510k Number | K864567 |
| Device Name: | 40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER |
| Classification | System, Balloon, Intra-aortic And Control |
| Applicant | ARIES MEDICAL, INC. TWO GILL ST. Woburn, MA 01801 |
| Contact | Michael L Rishton |
| Correspondent | Michael L Rishton ARIES MEDICAL, INC. TWO GILL ST. Woburn, MA 01801 |
| Product Code | DSP |
| CFR Regulation Number | 870.3535 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-11-19 |
| Decision Date | 1987-05-12 |