The following data is part of a premarket notification filed by Arrow Intl., Inc. with the FDA for 14 Fr Two-lumen Hemodialysis Catherization Kit With Blue Flextip Arrowg+ard Blue Catheter For High Volume Infusions, Pro.
| Device ID | K993933 |
| 510k Number | K993933 |
| Device Name: | 14 FR TWO-LUMEN HEMODIALYSIS CATHERIZATION KIT WITH BLUE FLEXTIP ARROWG+ARD BLUE CATHETER FOR HIGH VOLUME INFUSIONS, PRO |
| Classification | Catheter, Hemodialysis, Non-implanted |
| Applicant | ARROW INTL., INC. 2400 BERNVILLE RD. Reading, PA 19605 |
| Contact | Thomas D Nickel |
| Correspondent | Thomas D Nickel ARROW INTL., INC. 2400 BERNVILLE RD. Reading, PA 19605 |
| Product Code | MPB |
| CFR Regulation Number | 876.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-11-18 |
| Decision Date | 2000-09-14 |
| Summary: | summary |