Meloy Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Meloy Laboratories, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Meloy Laboratories, Inc. has 15 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 15 cleared submissions from 1977 to 1985. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Meloy Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Meloy Laboratories, Inc.
15 devices
Cleared
Jun 21, 1985
SS-A(RO) & SS-B(LA) ANTIBODY ASSAY
Immunology
43d
Cleared
Jan 04, 1985
MELOY LAB-ANTINUCLEAR ANTIBODY TEST-HEP-2 CELL CUL
Immunology
35d
Cleared
Jul 19, 1984
MELOY IMMUNOSTAT MONOCLONAL FACTOR VIII
Hematology
87d
Cleared
Jun 26, 1984
MELOY AUTOANTIBODY TEST SYS
Immunology
20d
Cleared
Jul 18, 1983
ANTI-ENA TEST
Immunology
89d
Cleared
Feb 12, 1982
ANA TEST (MOUSE LIVER SUBSTRATE)
Immunology
10d
Cleared
Jan 22, 1982
TOTAL HEMOLYTIC COMPLEMENT TEST KIT
Immunology
18d
Cleared
May 15, 1981
HUMAN IGG-ALBUMIN TEST KIT
Chemistry
17d
Cleared
Jan 16, 1980
IMMUNOSTAT TSH TEST
Chemistry
35d
Cleared
Sep 24, 1979
ANTI-NUCLEAR ANTIBODY TEST
Immunology
53d
Cleared
Jul 30, 1979
IMMUNOSPOT TSH TEST
Chemistry
48d
Cleared
Mar 15, 1979
ANTI-NATIVE DEOXYRIB-ONUCLEIC ACID ANTI
Immunology
37d