The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Cordis Brite Tip, Envoy Guiding Catheter.
| Device ID | K952185 |
| 510k Number | K952185 |
| Device Name: | CORDIS BRITE TIP, ENVOY GUIDING CATHETER |
| Classification | Catheter, Percutaneous |
| Applicant | CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Contact | Kevin Macdonald |
| Correspondent | Kevin Macdonald CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-05-09 |
| Decision Date | 1995-08-02 |