LCLUnclassified
Radioimmunoassay, Phencyclidine
Unknown
LCL is the FDA product code for Radioimmunoassay, Phencyclidine. As of , FDA records hold 11 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- LCL
- Device name
- Radioimmunoassay, Phencyclidine
- Device class
- Unclassified
- Review panel
- Unknown
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 11
- Ingested recalls
- 0
Clearances, product code LCL
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1980 | 1 |
| 1983 | 1 |
| 1987 | 1 |
| 1988 | 3 |
| 1989 | 1 |
| 1991 | 1 |
| 1999 | 1 |
| 2002 | 1 |
Applicants with the most clearances
Product code LCL| Applicant | Clearances |
|---|---|
| Abbott Medical | 2 |
| Hoffmann-La Roche, Inc. | 2 |
| Immunalysis Corporation | 2 |
| Syva Co. | 2 |
| Phamatech Inc. | 1 |
| Psychemedics Corp. | 1 |
| Roche Diagnostic Systems, Inc. | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
