Earl-Clay Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Earl-Clay Laboratories, Inc. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Earl-Clay Laboratories, Inc. has 21 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 21 cleared submissions from 1984 to 1986.
Browse the FDA 510(k) cleared devices submitted by Earl-Clay Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Earl-Clay Laboratories, Inc.
21 devices
Cleared
May 13, 1986
ULTRACLONE 01-2300 CELL LINE
Pathology
14d
Cleared
May 05, 1986
ULTRACLONE 01-700 CELL LINE
Pathology
7d
Cleared
Oct 31, 1985
ULTRACLONE 05-100 GUINEA PIG RBC
Pathology
15d
Cleared
Aug 12, 1985
ULTRACLONE ECL-01-2200 CELL LINE
Pathology
13d
Cleared
May 10, 1985
ULTRACLONE ECL-01-800 CELL LINE
Pathology
24d
Cleared
Oct 31, 1984
ULTRAXLONE ECL-01-1000 CELL LINE
Hematology
50d
Cleared
Oct 31, 1984
ULTRACLONE ECL-01-2100 CELL LINE
Hematology
50d
Cleared
Oct 31, 1984
ULTRACLONE ECL-01-1100
Hematology
50d
Cleared
Oct 17, 1984
ULTRACLONE ECL-01-900 CELL LINE
Pathology
15d
Cleared
Oct 17, 1984
ULTRACLONE ECL-01-1300 CELL LINE
Pathology
15d
Cleared
Oct 17, 1984
ULTRACLONE ECL-01-1400 CELL LINE
Pathology
15d
Cleared
May 11, 1984
ULTRACLONE ECL-01-800 CELL LINE
Hematology
39d