Ramco Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ramco Laboratories, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Ramco Laboratories, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1981 to 1998. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Ramco Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ramco Laboratories, Inc.
9 devices
Cleared
Oct 22, 1998
VFE
Hematology
48d
Cleared
Oct 21, 1998
TFR
Immunology
202d
Cleared
Nov 29, 1991
EPO-RIA
Hematology
296d
Cleared
Sep 04, 1987
SPECTRO C
Hematology
39d
Cleared
Mar 30, 1987
VWF IMMUNOBLOT
Hematology
118d
Cleared
May 01, 1986
SPECTRO VWF
Hematology
34d
Cleared
Jun 22, 1983
PTH MR
Chemistry
47d
Cleared
Dec 28, 1982
CANDIDA DETECTION SYSTEM
Microbiology
77d
Cleared
Aug 12, 1981
SPECTRO FEIRITIN
Microbiology
22d