Immulok, Inc.
Mchenry, IL, US
Immulok, Inc. appears in FDA device records in Mchenry, IL. FDA records list 15 510(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
- 15
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 15 510(k) clearances for Immulok, Inc. between 1981 and 1983. The busiest year on record is 1982, with 9. The most recent is 1983, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 3 |
| 1982 | 9 |
| 1983 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K830971 | HERPES SIMPLEX VIRUS TYPING REAGENTS | GQL | Substantially Equivalent | |
| K830342 | CULUTURE SET CHLAMYDIA ISOLATION AND | LKI | Substantially Equivalent | |
| K830250 | CVT VIRAL TRANSPORTS | JTW | Substantially Equivalent | |
| K823304 | RIASET PROLACTIN RIA KIT | CFT | Substantially Equivalent | |
| K822785 | FLUOROSET IMMUNOFLUORESCENT ANTIBODY | GQL | Substantially Equivalent | |
| K823055 | FLOUROSET IMMUNOFLUORESCENT ANTIBODY | DHN | Substantially Equivalent | |
| K822606 | CYTOMEGALOVIRUS ANTOBODY IGG | LIN | Substantially Equivalent | |
| K822605 | TOXOPLASMA GONDII ANTIBODY IGG | LJK | Substantially Equivalent | |
| K822607 | ANTINUCLEAR ANTOBODY CELL SUBSTRATE | DHN | Substantially Equivalent | |
| K821567 | IMMULOK CULTURESET | GQL | Substantially Equivalent | |
| K821411 | HISTOSET IMMUNOPEROFIDASE TISSUE | GQL | Substantially Equivalent | |
| K820390 | HISTOSET IMMUNOPEROXIDASE TISSURE KIT | LKH | Substantially Equivalent | |
| K812821 | H-103 IGG, H-104 IGA, H-105 IGM | DFZ | Substantially Equivalent | |
| K812497 | IMMULIK STAIN PLATE | IEG | Substantially Equivalent | |
| K811721 | H-101 KAPPA,H-102 LAMBDA,H-107 LYSOZME | DFH | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- DHNAntinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
- LINAntisera, Conjugated Fluorescent, Cytomegalovirus
- LKIAntisera, Fluorescent, Chlamydia Spp.
- GQLAntisera, Fluorescent, Herpesvirus Hominis 1,2
- LJKAntisera, If, Toxoplasma Gondii
- LKHAntisera, Immunoperoxidase, Chlamydia Spp.
- DFZIgg (Gamma Chain Specific), Antigen, Antiserum, Control
- DFHKappa, Antigen, Antiserum, Control
- CFTRadioimmunoassay, Prolactin (Lactogen)
- JTWSystem, Transport, Aerobic
- IEGTable, Slide Warming
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