DPA
5 FDA 510(k) clearances · Product code
77 daysmedian time to decision
182 days90th percentile
5clearances measured
FDA profile
- Official device name
- Apparatus, General Use, Thin Layer Chromatography
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.2270
- Medical specialty
- Clinical Chemistry
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| DE-TOX TUBES A AND DE-TOX TUBES B (K904326) | Dyna-Tek Industries | 1991-01-17 |
| CHROMATOGRAPHY KIT (K884176) | Gelman Sciences, Inc. | 1989-04-04 |
| TECHNICON FAST-LC SYS. FOR THEOPHYLLINE (K791431) | Technicon Instruments Corp. | 1979-10-11 |
| REAGENT SET, RENORPACE (K770765) | G.D. Searle and Co. | 1977-06-24 |
| MINIATURE ASCENDING PAPER CHROMATO- (K760908) | Ackerman Nuclear, Inc. | 1976-11-19 |
Track DPA automatically
Every clearance here is in the API, with alerts when new ones post.