DFG — Lambda, Rhodamine, Antigen, Antiserum, Control Class II
FDA product code DFG covers "Lambda, Rhodamine, Antigen, Antiserum, Control", a Class II medical device regulated under 21 CFR 866.5550. Submissions are reviewed by the Immunology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- DFG
- Device Class
- Class II
- Regulation Number
- 866.5550
- Submission Type
- Review Panel
- IM
- Medical Specialty
- Immunology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K023368 | aortech critical care | TRUCATH.IP | October 28, 2002 |