KTA — Medium, Contrast, Radiologic Class U
FDA product code KTA covers "Medium, Contrast, Radiologic", a Class U medical device. Submissions are reviewed by the Unknown panel. At least 8 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- KTA
- Device Class
- Class U
- Regulation Number
- Submission Type
- Review Panel
- RA
- Medical Specialty
- Unknown
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K800843 | medefield pty. | MEDEFIZZ A & MEDEFIZZ B | June 17, 1980 |
| K800840 | medefield pty. | MEDEFOAM-2 | June 17, 1980 |
| K800844 | medefield pty. | MEDEBAR XL | May 30, 1980 |
| K800459 | central pharmaceuticals | BARIUM SULFATE, USP IN SUSPENSION | May 30, 1980 |
| K800839 | medefield pty. | MEDESCAN | May 30, 1980 |
| K800841 | medefield pty. | MEDEBAR M | May 30, 1980 |
| K800842 | medefield pty. | MEDEBAR XAC-90 | May 30, 1980 |
| K760736 | c.r. bard | BARIMEX, BARIUM SULFATE COMPOUND | November 9, 1976 |