Corning Costar Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Corning Costar Corp. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Corning Costar Corp. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1980 to 1987.
Browse the FDA 510(k) cleared devices submitted by Corning Costar Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Corning Costar Corp.
8 devices
Cleared
May 15, 1987
CELL LIFTER
Microbiology
23d
Cleared
May 06, 1986
U - STAR (MICRO-STAR)
General Hospital
69d
Cleared
Dec 03, 1982
OCTAPETTES
Hematology
39d
Cleared
Nov 29, 1982
CELL SCRAPER
Hematology
35d
Cleared
Feb 02, 1981
ASSAY STRIPS
Microbiology
41d
Cleared
Jan 28, 1981
SEROCLUSTER EIA PLATES
Immunology
36d
Cleared
Jan 28, 1981
SEROCLUSTER FLEXIBLE VINYL U & V PL.
Immunology
36d
Cleared
Feb 13, 1980
SEROCLUSTER U AND V
Microbiology
8d