DPA — Apparatus, General Use, Thin Layer Chromatography Class I
FDA product code DPA covers "Apparatus, General Use, Thin Layer Chromatography", a Class I medical device regulated under 21 CFR 862.2270. Submissions are reviewed by the Clinical Chemistry panel. At least 5 recent 510(k) clearances have been granted under this product code.
Classification details
- Product Code
- DPA
- Device Class
- Class I
- Regulation Number
- 862.2270
- Submission Type
- 510(k) Exempt
- Review Panel
- TX
- Medical Specialty
- Clinical Chemistry
- Implant
- No
Recent 510(k) clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K904326 | Dyna-Tek Industries | DE-TOX TUBES A AND DE-TOX TUBES B | Jan 17, 1991 |
| K884176 | Gelman Sciences | CHROMATOGRAPHY KIT | Apr 4, 1989 |
| K791431 | Technicon Instruments | TECHNICON FAST-LC SYS. FOR THEOPHYLLINE | Oct 11, 1979 |
| K770765 | G.D. Searle And | REAGENT SET, RENORPACE | Jun 24, 1977 |
| K760908 | Ackerman Nuclear | MINIATURE ASCENDING PAPER CHROMATO- | Nov 19, 1976 |