Health Development Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Health Development Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Health Development Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1980 to 1983. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Health Development Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Health Development Corp.
5 devices
Cleared
Apr 12, 1983
PEM-C
Microbiology
64d
Cleared
Feb 24, 1983
SEMINAL COLLECTION DEVICE
Obstetrics & Gynecology
57d
Cleared
Mar 04, 1981
PERCUTANEOUS GASTROINTESTINAL TUBE
Gastroenterology & Urology
8d
Cleared
Oct 31, 1980
KEOFEED (R) EASY-FILL ENTERIC FEED BAG
Gastroenterology & Urology
24d
Cleared
Jan 16, 1980
SURGIFEED
Gastroenterology & Urology
139d