GIE — Fibrometer Class II
FDA Device Classification
Classification Details
- Product Code
- GIE
- Device Class
- Class II
- Regulation Number
- 864.5400
- Submission Type
- Review Panel
- HE
- Medical Specialty
- Hematology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K820532 | american scientific products | DISPO FIBRIN PIPET TIPS B4182-2 | April 8, 1982 |
| K820533 | american scientific products | B4182-1 | April 8, 1982 |