Serono Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Serono Laboratories, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Serono Laboratories, Inc. has 10 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1978 to 1984.
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 - Serono Laboratories, Inc.
10 devices
Cleared
Mar 02, 1984
ALDOSTERONE RADIOIMMUNOASSAY TEST KIT
Chemistry
78d
Cleared
Mar 31, 1981
ESTRIOL RADIOIMMUNOASSAY TEST KIT
Chemistry
15d
Cleared
Mar 27, 1981
HUMAN PLACENTAL LACTOGEN RADIOIMMUNO-
Chemistry
18d
Cleared
Oct 30, 1979
PAP-CHECK RIA KIT
Chemistry
18d
Cleared
May 23, 1979
ESTRADIOL RIA KIT
Chemistry
44d
Cleared
May 03, 1979
PROGESTERONE
Chemistry
57d
Cleared
Feb 22, 1979
RIA KIT, GLUCOSE
Chemistry
57d
Cleared
Jan 17, 1979
RIA KIT, NEONATAL T4
Chemistry
33d
Cleared
Dec 20, 1978
RIA KIT, PREG-STAT
Immunology
68d
Cleared
Aug 14, 1978
INSULIN RIA KIT
Immunology
19d