Intl. Immunoassay Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intl. Immunoassay Laboratories, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Intl. Immunoassay Laboratories, Inc. has 27 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 27 cleared submissions from 1980 to 1992.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intl. Immunoassay Laboratories, Inc.
27 devices
Cleared
Apr 22, 1992
MYDAS(TM)-MB2/MYDAS(TM)-MB
Chemistry
268d
Cleared
Oct 23, 1991
STAMBI-CK
Chemistry
89d
Cleared
Jul 08, 1991
PROPOSED NEW USE OF INSTRUMENT SYSTEM AND TEST KIT
Chemistry
49d
Cleared
Nov 06, 1990
MYDAS(TM) BRAND SOLID-PHASE ANTIBODY REAGENTS
Chemistry
98d
Cleared
Sep 07, 1990
LABELLING CHANGES TO IMPRES-MB-X
Chemistry
38d
Cleared
May 15, 1990
MODIFIED LABEL FOR EMBRIA-CK, QUICK-MB/MICROMI-MB
Chemistry
48d
Cleared
Mar 16, 1989
IMPRES-MB (ADDITION OF AN OPTIONAL TEST PROCEDURE)
Chemistry
37d
Cleared
Mar 13, 1989
IMPRES-MB REAGENT A AND REAGENT B
Chemistry
38d
Cleared
Oct 31, 1988
IMMUNOCCULT-LXI
Hematology
77d
Cleared
Sep 30, 1988
ISOFOR-MM (TM)
Chemistry
63d
Cleared
Sep 30, 1988
CHECK-MM
Chemistry
63d
Cleared
Jul 08, 1988
IMMUNOCCULT EIA TEST KIT
Hematology
473d