KJG — Tube, Tissue Culture Class I
FDA product code KJG covers "Tube, Tissue Culture", a Class I medical device regulated under 21 CFR 864.3010. Submissions are reviewed by the Pathology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- KJG
- Device Class
- Class I
- Regulation Number
- 864.3010
- Submission Type
- Review Panel
- PA
- Medical Specialty
- Pathology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K823747 | corning medical and scientific | 24 CELL WELLS TISSUE CULTURE | January 5, 1983 |