The following data is part of a premarket notification filed by Arrow International, Inc. with the FDA for Vectorflow; Antegrade Chronic Hemodialysis Catheter, Retrograde Chronic Hemodialysis Catheter, Retrograde Replacement Hu.
| Device ID | K141051 |
| 510k Number | K141051 |
| Device Name: | VECTORFLOW; ANTEGRADE CHRONIC HEMODIALYSIS CATHETER, RETROGRADE CHRONIC HEMODIALYSIS CATHETER, RETROGRADE REPLACEMENT HU |
| Classification | Catheter, Hemodialysis, Implanted |
| Applicant | ARROW INTERNATIONAL, INC. 2400 BERNVILLE RD. Reading, PA 19605 |
| Contact | Frank Pelc |
| Correspondent | Frank Pelc ARROW INTERNATIONAL, INC. 2400 BERNVILLE RD. Reading, PA 19605 |
| Product Code | MSD |
| CFR Regulation Number | 876.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-04-24 |
| Decision Date | 2014-07-07 |
| Summary: | summary |