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 |