Company ยท US
Clinetics Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1986. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 7, 1986 | K862180 | MODIFIED COTROPIN RADIOIMMUNOASSAY KIT Clinetics Corp. | CEP |
| Jan 18, 1985 | K844066 | COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH Clinetics Corp. | CGJ |
| Oct 22, 1984 | K841580 | TSH RECEPTOR ANTIBODY KIT 125I TSH Clinetics Corp. | JZO |
| Apr 4, 1984 | K833934 | ADRENOCORTICOTROPIC HORMONE TEST Clinetics Corp. | CKG |
| Mar 17, 1983 | K830357 | RADIOIMMUNOASSAY IMMUNOGLOBULINS D.E Clinetics Corp. | DGC |
| Dec 22, 1982 | K823380 | 125-I LH RADIOIMMUNOASSAY KIT Clinetics Corp. | CEP |
| Dec 22, 1982 | K823379 | 125-I FSH RADIOIMMUNOASSAY KIT Clinetics Corp. | CGJ |
| Sep 2, 1982 | K822152 | HCG BETA RIA KIT Clinetics Corp. | JHI |
| Sep 26, 1980 | K801306 | CLINETICS PCA COLUMN Clinetics Corp. | DHX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||