GHC — Tube, Sedimentation Rate Class I
FDA product code GHC covers "Tube, Sedimentation Rate", a Class I medical device regulated under 21 CFR 864.6700. Submissions are reviewed by the Hematology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- GHC
- Device Class
- Class I
- Regulation Number
- 864.6700
- Submission Type
- Review Panel
- HE
- Medical Specialty
- Hematology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K885114 | investigacion farmaceutica s.a. de c.v | SALMONELLA IFA* | August 15, 1989 |