The following data is part of a premarket notification filed by Cordis Neurovascular, Inc. with the FDA for Fg Infusion Catheter.
| Device ID | K971306 |
| 510k Number | K971306 |
| Device Name: | FG INFUSION CATHETER |
| Classification | Catheter, Continuous Flush |
| Applicant | CORDIS NEUROVASCULAR, INC. 14740 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Contact | Lisa Wells |
| Correspondent | Lisa Wells CORDIS NEUROVASCULAR, INC. 14740 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Product Code | KRA |
| CFR Regulation Number | 870.1210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-04-08 |
| Decision Date | 1997-07-14 |
| Summary: | summary |