Cytotech, Inc.
Cytotech, Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1988.
Top product codes for Cytotech, Inc.
Recent clearances by Cytotech, Inc.
- K882829 — CIRCULATING IMMUNE COMPLEXES CONTROLS
- K874379 — CIC-RAJI CELL REPLACEMENT ENZYME IMMUNOASSAY
- K873249 — ANTINUCLEAR ANTIBODY (ANA) POSITIVE CONTROLS
- K872426 — CYTOTECH C1-INHIBITOR ENZYME IMMUNOASSAY
- K871801 — CYTOTECH ANTINUCLEAR ANTIBODY (ANA) IFA KIT
- K864315 — CYTOTECH RUBELLA IGG ENZYME IMMUNOASSAY
- K862838 — CYTOTECH HSV IGG ENZYME IMMUNOASSAY
- K863363 — CYTOTECH TOXOPLASMA IGG ENZYME IMMUNOASSAY
- K862649 — CYTOTECH CIC ENZYME IMMUNOASSAY
- K860493 — CYTOTECH CMV IGG EIA
Data sourced from openFDA. This site is unofficial and independent of the FDA.