The following data is part of a premarket notification filed by Cook Incorporated with the FDA for Cook Unimpregnated Central Venous Catheter.
| Device ID | K182252 |
| 510k Number | K182252 |
| Device Name: | Cook Unimpregnated Central Venous Catheter |
| Classification | Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days |
| Applicant | Cook Incorporated 750 Daniels Way Bloomington, IN 47404 |
| Contact | Johnathan Liu |
| Correspondent | Chelsea Woods Cook Incorporated 750 Daniels Way P.Box 489 Bloomington, IN 47402 |
| Product Code | FOZ |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-08-20 |
| Decision Date | 2019-05-17 |
| Summary: | summary |