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 |