The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Vista Brite Tip Catheters.
| Device ID | K992673 |
| 510k Number | K992673 |
| Device Name: | VISTA BRITE TIP CATHETERS |
| Classification | Catheter, Percutaneous |
| Applicant | CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Contact | Dennis S Griffin |
| Correspondent | Dennis S Griffin 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 | 1999-08-10 |
| Decision Date | 1999-10-12 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20705032019115 | K992673 | 000 |
| 20705032019177 | K992673 | 000 |
| 20705032042953 | K992673 | 000 |
| 20705032031322 | K992673 | 000 |
| 20705032031360 | K992673 | 000 |
| 20705032043813 | K992673 | 000 |
| 20705032063835 | K992673 | 000 |
| 20705032063842 | K992673 | 000 |
| 20705032063859 | K992673 | 000 |
| 20705032072691 | K992673 | 000 |
| 20705032072707 | K992673 | 000 |
| 20705032053454 | K992673 | 000 |
| 20705032053461 | K992673 | 000 |
| 20705032031506 | K992673 | 000 |
| 20705032053447 | K992673 | 000 |
| 20705032019078 | K992673 | 000 |
| 20705032019092 | K992673 | 000 |
| 20705032019054 | K992673 | 000 |