Dilab, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dilab, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Dilab, Inc. has 11 FDA 510(k) cleared chemistry devices. Based in Miami, US.
Historical record: 11 cleared submissions from 1985 to 1987.
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 - Dilab, Inc.
11 devices
Cleared
Apr 21, 1987
RAPID AS LATEX
Microbiology
293d
Cleared
Jun 26, 1985
ALBUMIN
Chemistry
111d
Cleared
Jun 25, 1985
CREATININE
Chemistry
110d
Cleared
Jun 25, 1985
URIC ACID
Chemistry
110d
Cleared
Jun 25, 1985
PHOSPHORUS
Chemistry
110d
Cleared
Jun 25, 1985
TOTAL PROTEINS
Chemistry
110d
Cleared
Jun 25, 1985
CHOLESTEROL
Chemistry
110d
Cleared
Jun 10, 1985
CALCIUM
Chemistry
95d
Cleared
Jun 10, 1985
GLUCOSE
Chemistry
95d
Cleared
Jun 10, 1985
CHLORIDE
Chemistry
95d
Cleared
Jun 10, 1985
UREA
Chemistry
95d