NUTRICATH
Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days
EXCO, INC.
The following data is part of a premarket notification filed by Exco, Inc. with the FDA for Nutricath.
Pre-market Notification Details
| Device ID | K813374 |
| 510k Number | K813374 |
| Device Name: | NUTRICATH |
| Classification | Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days |
| Applicant | EXCO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FOZ |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-01 |
| Decision Date | 1982-03-15 |
Trademark Results [NUTRICATH]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NUTRICATH 74069491 not registered Dead/Abandoned |
Societe Vygon 1990-06-15 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.