Cytotech, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cytotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CIRCULATING IMMUNE COMPLEXES CONTROLS, CIC-RAJI CELL REPLACEMENT ENZYME IMMUNOASSAY, ANTINUCLEAR ANTIBODY (ANA) POSITIVE CONTROLS
10
Total
10
Cleared
0
Denied
Cytotech, Inc. has 10 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 10 cleared submissions from 1986 to 1988. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Cytotech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cytotech, Inc.
10 devices
Cleared
Aug 04, 1988
CIRCULATING IMMUNE COMPLEXES CONTROLS
Immunology
27d
Cleared
Nov 25, 1987
CIC-RAJI CELL REPLACEMENT ENZYME IMMUNOASSAY
Immunology
30d
Cleared
Sep 22, 1987
ANTINUCLEAR ANTIBODY (ANA) POSITIVE CONTROLS
Immunology
36d
Cleared
Jul 23, 1987
CYTOTECH C1-INHIBITOR ENZYME IMMUNOASSAY
Immunology
31d
Cleared
Jun 09, 1987
CYTOTECH ANTINUCLEAR ANTIBODY (ANA) IFA KIT
Immunology
32d
Cleared
Feb 02, 1987
CYTOTECH RUBELLA IGG ENZYME IMMUNOASSAY
Microbiology
91d
Cleared
Dec 09, 1986
CYTOTECH HSV IGG ENZYME IMMUNOASSAY
Microbiology
137d
Cleared
Nov 13, 1986
CYTOTECH TOXOPLASMA IGG ENZYME IMMUNOASSAY
Microbiology
72d
Cleared
Sep 04, 1986
CYTOTECH CIC ENZYME IMMUNOASSAY
Immunology
55d
Cleared
May 20, 1986
CYTOTECH CMV IGG EIA
Microbiology
99d