Bioclinical Group
Walker, MI, US
Bioclinical Group appears in FDA device records in Walker, MI. 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 Bioclinical Group between 1982 and 1986. The busiest year on record is 1982, with 6. The most recent is 1986, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 6 |
| 1983 | 1 |
| 1985 | 1 |
| 1986 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K862968 | FREE T3 RADIOIMMUNOASSAY KIT | KHQ | Substantially Equivalent | |
| K853837 | LH/FSH RADIOIMMUNOASSAY KIT | CEP | Substantially Equivalent | |
| K832638 | CORTISOL RADIOIMMUNOASSAY KIT | CGR | Substantially Equivalent | |
| K823005 | BIO MAG FREE T4 RADIOIMMUNOASSAY KIT | CEC | Substantially Equivalent | |
| K823004 | BIO MAG TOTAL T4 RADIOIMMUNOASSAY KIT | CDX | Substantially Equivalent | |
| K822840 | RADIOIMMUNOASSAY, HUMAN CHORRIONIC | JHI | Substantially Equivalent | |
| K822515 | B-HCG RADIOIMMUNOASSAY KIT | JHI | Substantially Equivalent | |
| K821241 | FREE T4 RADIOIMMUNOASSAY KIT | CEC | Substantially Equivalent | |
| K821101 | TOTAL RADIOIMMUNOASSAY KIT | CDX | 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