# Immunotech Corp.

- Location (FDA's records): Boston, MA
- FDA decisions: 42 (1980–2019): 42 510(k) clearances
- Names in FDA's records: Immunotech Corp. (37); Immunotech, Inc. (3); Immunotech S.A. (1); Immunotech S.R.O. (1)
- Product codes: GKZ (6), CDP (3), JLW (3), CEE (2), CEC (2), CDX (2), CGI (2), KLS (2), KXT (2), CGR (1), DJG (1), LCW (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Diagnostic Systems Laboratories, Inc.: 1 (https://510kreport.com/company/diagnostic-systems-laboratories)

## Recent decisions
- K191350: ACTIVE® Free Testosterone RIA (Dec 20, 2019)
- K954188: Opticlone IGG1 Fitc/IGG2A PE Isotypic Control (Nov 3, 1995)
- K946335: Opticlone (TM CD3 Fitc/CD19 PE Monoclonal Antibodies (Oct 20, 1995)
- K953498: Opticlone IGG1 Fitc/IGG1 PE Isotypic Control (Sep 8, 1995)
- K952789: Opticlone CD4FITC/CD8 PE Monoclonal Antibodies (Aug 14, 1995)
- K952182: Opticlone CD3/CD8 Monoclonal Antibodies (Jul 5, 1995)
- K950626: Opticlone CD3/CD4 Monoclonal Antibodies (May 5, 1995)
- K934012: FT4 Radioimmunoassay (Nov 16, 1993)

Source page: https://510kreport.com/company/immunotech
