The following data is part of a premarket notification filed by Arrow Intl., Inc. with the FDA for 8 Fr.-30cc Narrowflex Intra-aortic Balloon Catheter,.
| Device ID | K963920 |
| 510k Number | K963920 |
| Device Name: | 8 FR.-30CC NARROWFLEX INTRA-AORTIC BALLOON CATHETER, |
| Classification | System, Balloon, Intra-aortic And Control |
| Applicant | ARROW INTL., INC. 3000 BERNVILLE RD. Reading, PA 19605 |
| Contact | Thomas D Nickel |
| Correspondent | Thomas D Nickel ARROW INTL., INC. 3000 BERNVILLE RD. Reading, PA 19605 |
| Product Code | DSP |
| CFR Regulation Number | 870.3535 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-09-30 |
| Decision Date | 1997-06-17 |
| Summary: | summary |