Clinetics Corp.
Mchenry, IL, US
Clinetics Corp. appears in FDA device records in Mchenry, IL. FDA records list 9 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Clinetics Corp. between 1980 and 1986. The busiest year on record is 1982, with 3. The most recent is 1986, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1982 | 3 |
| 1983 | 1 |
| 1984 | 2 |
| 1985 | 1 |
| 1986 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K862180 | MODIFIED COTROPIN RADIOIMMUNOASSAY KIT | CEP | Substantially Equivalent | |
| K844066 | COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH | CGJ | Substantially Equivalent | |
| K841580 | TSH RECEPTOR ANTIBODY KIT 125I TSH | JZO | Substantially Equivalent | |
| K833934 | ADRENOCORTICOTROPIC HORMONE TEST | CKG | Substantially Equivalent | |
| K830357 | RADIOIMMUNOASSAY IMMUNOGLOBULINS D.E | DGC | Substantially Equivalent | |
| K823380 | 125-I LH RADIOIMMUNOASSAY KIT | CEP | Substantially Equivalent | |
| K823379 | 125-I FSH RADIOIMMUNOASSAY KIT | CGJ | Substantially Equivalent | |
| K822152 | HCG BETA RIA KIT | JHI | Substantially Equivalent | |
| K801306 | CLINETICS PCA COLUMN | DHX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain