Dyn-A-Med Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dyn-A-Med Products - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Dyn-A-Med Products has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1980 to 1984. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dyn-A-Med Products Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dyn-A-Med Products
5 devices
Cleared
Dec 17, 1984
CLAMP, TUBING, LINE
Gastroenterology & Urology
55d
Cleared
Dec 29, 1981
GEL ELECTRODE
Cardiovascular
47d
Cleared
May 27, 1981
BLADE, TONGUE
General & Plastic Surgery
29d
Cleared
Nov 24, 1980
PLASTIC ADHESIVE BANDAGE
General & Plastic Surgery
20d
Cleared
Oct 31, 1980
SPATULA, CERVICAL CYTOLOGICAL CYTOLOGY
Obstetrics & Gynecology
57d