Clinetics Corp.
FDA 510(k) & PMA Approved Devices — 9 products
Advertisement
Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K862180 | MODIFIED COTROPIN RADIOIMMUNOASSAY KIT | CEP | 1986-07-07 | View |
| 510(k) | K844066 | COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH | CGJ | 1985-01-18 | View |
| 510(k) | K841580 | TSH RECEPTOR ANTIBODY KIT 125I TSH | JZO | 1984-10-22 | View |
| 510(k) | K833934 | ADRENOCORTICOTROPIC HORMONE TEST | CKG | 1984-04-04 | View |
| 510(k) | K830357 | RADIOIMMUNOASSAY IMMUNOGLOBULINS D.E | DGC | 1983-03-17 | View |
| 510(k) | K823380 | 125-I LH RADIOIMMUNOASSAY KIT | CEP | 1982-12-22 | View |
| 510(k) | K823379 | 125-I FSH RADIOIMMUNOASSAY KIT | CGJ | 1982-12-22 | View |
| 510(k) | K822152 | HCG BETA RIA KIT | JHI | 1982-09-02 | View |
| 510(k) | K801306 | CLINETICS PCA COLUMN | DHX | 1980-09-26 | View |
No matching devices.
Advertisement