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 |