DKG — Plate, Cellulose, Tlc Class I
FDA product code DKG covers "Plate, Cellulose, Tlc", a Class I medical device regulated under 21 CFR 862.2270. Submissions are reviewed by the Clinical Chemistry panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- DKG
- Device Class
- Class I
- Regulation Number
- 862.2270
- Submission Type
- Review Panel
- TX
- Medical Specialty
- Clinical Chemistry
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K894327 | syva | EMIT D.A.U. LOW & MEDIUM CALIBRATOR A | August 3, 1989 |