GBP — Catheter, Multiple Lumen Class I
FDA Device Classification
Classification Details
- Product Code
- GBP
- Device Class
- Class I
- Regulation Number
- 878.4200
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K844889 | goosen enterprises | MENSINK-GOOSEN CATHETER | March 18, 1985 |
| K821220 | clincal instruments | MULTILUMEN INTRAVENOUS INFUSION CATHETER | July 9, 1982 |
| K820446 | dlp | CATHETER, MULTIPLE LUMEN | March 11, 1982 |