CHOClass II
Radioimmunoassay, Cyclic Amp
21 CFR 862.1230 / Clinical Chemistry
CHO is the FDA product code for Radioimmunoassay, Cyclic Amp, a class II device type, regulated under 21 CFR 862.1230. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- CHO
- Device name
- Radioimmunoassay, Cyclic Amp
- Regulation
- 21 CFR 862.1230
- Device class
- Class II
- Review panel
- Clinical Chemistry
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 6
- Ingested recalls
- 0
Clearances, product code CHO
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1981 | 2 |
| 1983 | 1 |
| 1984 | 1 |
| 1985 | 1 |
| 1986 | 1 |
Applicants with the most clearances
Product code CHO| Applicant | Clearances |
|---|---|
| Immuno Nuclear Corp. | 2 |
| Amersham Corp. | 1 |
| BD Becton Dickinson Vacutainer Systems Preanalytic | 1 |
| King Diagnostics, Inc. | 1 |
| New England Nuclear | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeNo registered establishment in MDM’s records lists product code CHO.
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