Medical Engineering and Development Institute is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Engineering and Development Institute - FDA 510(k) Cleared De...
6
Total
5
Cleared
0
Denied
Medical Engineering and Development Institute has 5 FDA 510(k) cleared medical devices. Based in West Lafayette, US.
Historical record: 5 cleared submissions from 1989 to 1990. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medical Engineering and Development Institute Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Engineering and Development Institute
6 devices
Cleared
Aug 24, 1990
WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL SET
Cardiovascular
81d
Cleared
Aug 23, 1990
BYRD DILATOR SHEATH SET - TEFLON
Cardiovascular
80d
Cleared
Aug 07, 1990
BYRD STAINLESS STEEL DILATOR
General & Plastic Surgery
63d
Cleared
Apr 17, 1990
LIFE-LINE(TM) VASCULAR ACCESS SYSTEM
General Hospital
252d
Cleared
Jun 23, 1989
BYRD EXTRACTOR SET
General & Plastic Surgery
50d
Cleared
Mar 22, 1989
LOCKING WIRE GUIDE STYLET
General & Plastic Surgery
33d